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My Organizations' Clinical Trials

Showing 25 of 25 entries

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Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Preserve Femoral Stem

Phase: N/A Priority: Normal

NCT ID: NCT03865667 Org: User:

Start: 01/15/19 End: 01/01/32 Due: 01/01/33

PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular Components

Phase: N/A Priority: Normal

NCT ID: NCT02823834 Org: User:

Start: 06/16/17 End: 06/30/27 Due: 06/30/28

Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Z Revision Femoral Stems

Phase: N/A Priority: Normal

NCT ID: NCT04064008 Org: User:

Start: 04/04/19 End: 04/30/30 Due: 04/30/31

Post Market Clinical Follow-up Study Protocol for PROFEMUR® Xm Femoral Stems

Phase: N/A Priority: Normal

NCT ID: NCT02309593 Org: User:

Start: 12/31/14 End: 12/21/21 Due: 12/21/22

Post Market Clinical Follow-Up Study Protocol for PROFEMUR® TL Modular Femoral Stems

Phase: N/A Priority: Normal

NCT ID: NCT02239783 Org: User:

Start: 11/30/14 End: 11/30/28 Due: 11/30/29

Post Market Clinical Follow-Up Study Protocol for PROCOTYL® C Acetabular Components

Phase: N/A Priority: Normal

NCT ID: NCT03576573 Org: User:

Start: 03/27/19 End: 12/31/32 Due: 12/31/33

Post Market Clinical Follow-Up Study Protocol for CONSERVE® Press-Fit Femoral Components

Phase: N/A Priority: Normal

NCT ID: NCT02285842 Org: User:

Start: 12/31/14 End: 12/31/28 Due: 12/31/29

CONSERVE Plus Post-Approval Study (PAS)

Phase: N/A Priority: Normal

NCT ID: NCT01367899 Org: User:

Start: 11/30/10 End: 09/30/14 Due: 09/30/15

PMCF Study for PROFEMUR® Am Femoral Components and PROCOTYL® O HA Coated Acetabular Components

Phase: N/A Priority: Normal

NCT ID: NCT02507258 Org: User:

Start: 12/31/17 End: 12/31/28 Due: 12/31/29

Wright Medical Technology Metal-on-Metal 522 Post-Market Surveillance Study

Phase: N/A Priority: Normal

NCT ID: NCT03450733 Org: User:

Start: 04/11/18 End: 06/18/22 Due: 06/18/23

Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator HA Coated Modular Femoral Stems

Phase: N/A Priority: Normal

NCT ID: NCT02314611 Org: User:

Start: 12/31/14 End: 11/30/23 Due: 11/30/24

Post Market Clinical Follow-Up Study for PROFEMUR® Preserve Classic Femoral Stem

Phase: N/A Priority: Normal

NCT ID: NCT04147559 Org: User:

Start: 10/21/20 End: 11/01/33 Due: 11/01/34

Post Market Clinical Follow-Up Study- EVOLUTION® Revision CCK

Phase: N/A Priority: Normal

NCT ID: NCT04145401 Org: User:

Start: 09/30/20 End: 11/01/33 Due: 11/01/34

Evaluation of Bone Mineral Density Changes After Total Hip Replacement: A Two-Year Clinical and DXA Analysis

Phase: N/A Priority: Normal

NCT ID: NCT02865447 Org: User:

Start: 03/09/17 End: 08/24/20 Due: 08/24/21

Post Market Clinical Follow-Up Study for EVOLUTION® BIOFOAM® Tibia and EVOLUTION® CS/CR Porous Femur

Phase: N/A Priority: Normal

NCT ID: NCT04301622 Org: User:

Start: 02/03/20 End: 08/31/32 Due: 08/31/33

EVOLUTION® Revision STEMMED CS Post Market Clinical Follow-up Study Protocol

Phase: N/A Priority: Normal

NCT ID: NCT06142669 Org: User:

Start: 10/31/23 End: 12/31/36 Due: 12/31/37

Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator Cemented Femoral Stems

Phase: N/A Priority: Normal

NCT ID: NCT02397746 Org: User:

Start: 07/31/15 End: 12/20/21 Due: 12/20/22

Radiostereometric Analysis (RSA) of the PROFEMUR® Preserve Classic Femoral Components

Phase: N/A Priority: Normal

NCT ID: NCT02668211 Org: User:

Start: 11/30/16 End: 12/31/19 Due: 12/31/20

Gait and Functional Outcomes Study Following Total Knee Arthroplasty With Medial-pivot or Posterior-stabilized Implants

Phase: N/A Priority: Normal

NCT ID: NCT02589197 Org: User:

Start: 07/13/16 End: 09/30/22 Due: 09/30/23

Post Market Clinical Follow-up Study Protocol for DYNASTY® BioFoam® Acetabular Components

Phase: N/A Priority: Normal

NCT ID: NCT02149667 Org: User:

Start: 12/31/14 End: 12/31/28 Due: 12/31/29

Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate Sacrificing Insert

Phase: N/A Priority: Normal

NCT ID: NCT04816773 Org: User:

Start: 01/27/22 End: 01/31/35 Due: 01/31/36

Post Market Clinical Follow-Up Study for MicroPort PROFEMUR® Preserve Classic Femoral Stem

Phase: N/A Priority: Normal

NCT ID: NCT04615039 Org: User:

Start: 12/31/21 End: 12/31/33 Due: 12/31/34

Ceramic on Metal Total Hip Replacement System Multi-Center,Investigational Device Exemption Clinical Trial

Phase: N/A Priority: Normal

NCT ID: NCT00820443 Org: User:

Start: 06/30/07 End: 10/31/13 Due: 10/31/14

Post Market Follow-Up Study of the EVOLUTION® Total Knee Arthroplasty System With Cruciate Sacrificing Inserts

Phase: N/A Priority: Normal

NCT ID: NCT02351414 Org: User:

Start: 06/15/15 End: 12/31/28 Due: 12/31/29

Post Market Clinical Follow-Up Study Protocol for PROFEMUR® L Revision Femoral Stems

Phase: N/A Priority: Normal

NCT ID: NCT02314702 Org: User:

Start: 09/04/15 End: 10/31/27 Due: 10/31/28

Title	NCT ID	Organization	User	Status	Start Date	End Date	Reporting Due Date	Last Checked	User Role	Org Created
Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Preserve Femoral Stem	NCT03865667	MicroPort Orthopedics Inc.	user2@example.com	None	2019-01-15	2032-01-01	2033-01-01	-	-	2025-07-14
PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular Components	NCT02823834	MicroPort Orthopedics Inc.	user2@example.com	None	2017-06-16	2027-06-30	2028-06-30	-	-	2025-07-14
Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Z Revision Femoral Stems	NCT04064008	MicroPort Orthopedics Inc.	user2@example.com	None	2019-04-04	2030-04-30	2031-04-30	-	-	2025-07-14
Post Market Clinical Follow-up Study Protocol for PROFEMUR® Xm Femoral Stems	NCT02309593	MicroPort Orthopedics Inc.	user2@example.com	None	2014-12-31	2021-12-21	2022-12-21	-	-	2025-07-14
Post Market Clinical Follow-Up Study Protocol for PROFEMUR® TL Modular Femoral Stems	NCT02239783	MicroPort Orthopedics Inc.	user2@example.com	None	2014-11-30	2028-11-30	2029-11-30	-	-	2025-07-14
Post Market Clinical Follow-Up Study Protocol for PROCOTYL® C Acetabular Components	NCT03576573	MicroPort Orthopedics Inc.	user2@example.com	None	2019-03-27	2032-12-31	2033-12-31	-	-	2025-07-14
Post Market Clinical Follow-Up Study Protocol for CONSERVE® Press-Fit Femoral Components	NCT02285842	MicroPort Orthopedics Inc.	user2@example.com	None	2014-12-31	2028-12-31	2029-12-31	-	-	2025-07-14
CONSERVE Plus Post-Approval Study (PAS)	NCT01367899	MicroPort Orthopedics Inc.	user2@example.com	None	2010-11-30	2014-09-30	2015-09-30	-	-	2025-07-14
PMCF Study for PROFEMUR® Am Femoral Components and PROCOTYL® O HA Coated Acetabular Components	NCT02507258	MicroPort Orthopedics Inc.	user2@example.com	None	2017-12-31	2028-12-31	2029-12-31	-	-	2025-07-14
Wright Medical Technology Metal-on-Metal 522 Post-Market Surveillance Study	NCT03450733	MicroPort Orthopedics Inc.	user2@example.com	None	2018-04-11	2022-06-18	2023-06-18	-	-	2025-07-14
Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator HA Coated Modular Femoral Stems	NCT02314611	MicroPort Orthopedics Inc.	user2@example.com	None	2014-12-31	2023-11-30	2024-11-30	-	-	2025-07-14
Post Market Clinical Follow-Up Study for PROFEMUR® Preserve Classic Femoral Stem	NCT04147559	MicroPort Orthopedics Inc.	user2@example.com	None	2020-10-21	2033-11-01	2034-11-01	-	-	2025-07-14
Post Market Clinical Follow-Up Study- EVOLUTION® Revision CCK	NCT04145401	MicroPort Orthopedics Inc.	user2@example.com	None	2020-09-30	2033-11-01	2034-11-01	-	-	2025-07-14
Evaluation of Bone Mineral Density Changes After Total Hip Replacement: A Two-Year Clinical and DXA Analysis	NCT02865447	MicroPort Orthopedics Inc.	user2@example.com	None	2017-03-09	2020-08-24	2021-08-24	-	-	2025-07-14
Post Market Clinical Follow-Up Study for EVOLUTION® BIOFOAM® Tibia and EVOLUTION® CS/CR Porous Femur	NCT04301622	MicroPort Orthopedics Inc.	user2@example.com	None	2020-02-03	2032-08-31	2033-08-31	-	-	2025-07-14
EVOLUTION® Revision STEMMED CS Post Market Clinical Follow-up Study Protocol	NCT06142669	MicroPort Orthopedics Inc.	user2@example.com	None	2023-10-31	2036-12-31	2037-12-31	-	-	2025-07-14
Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator Cemented Femoral Stems	NCT02397746	MicroPort Orthopedics Inc.	user2@example.com	None	2015-07-31	2021-12-20	2022-12-20	-	-	2025-07-14
Radiostereometric Analysis (RSA) of the PROFEMUR® Preserve Classic Femoral Components	NCT02668211	MicroPort Orthopedics Inc.	user2@example.com	None	2016-11-30	2019-12-31	2020-12-31	-	-	2025-07-14
Gait and Functional Outcomes Study Following Total Knee Arthroplasty With Medial-pivot or Posterior-stabilized Implants	NCT02589197	MicroPort Orthopedics Inc.	user2@example.com	None	2016-07-13	2022-09-30	2023-09-30	-	-	2025-07-14
Post Market Clinical Follow-up Study Protocol for DYNASTY® BioFoam® Acetabular Components	NCT02149667	MicroPort Orthopedics Inc.	user2@example.com	None	2014-12-31	2028-12-31	2029-12-31	-	-	2025-07-14
Post Market Clinical Follow-Up Study for EVOLUTION® NitrX™ Keeled Tibia and EVOLUTION® NitrX™ CS/CR Femur With Cruciate Sacrificing Insert	NCT04816773	MicroPort Orthopedics Inc.	user2@example.com	None	2022-01-27	2035-01-31	2036-01-31	-	-	2025-07-14
Post Market Clinical Follow-Up Study for MicroPort PROFEMUR® Preserve Classic Femoral Stem	NCT04615039	MicroPort Orthopedics Inc.	user2@example.com	None	2021-12-31	2033-12-31	2034-12-31	-	-	2025-07-14
Ceramic on Metal Total Hip Replacement System Multi-Center,Investigational Device Exemption Clinical Trial	NCT00820443	MicroPort Orthopedics Inc.	user2@example.com	None	2007-06-30	2013-10-31	2014-10-31	-	-	2025-07-14
Post Market Follow-Up Study of the EVOLUTION® Total Knee Arthroplasty System With Cruciate Sacrificing Inserts	NCT02351414	MicroPort Orthopedics Inc.	user2@example.com	None	2015-06-15	2028-12-31	2029-12-31	-	-	2025-07-14
Post Market Clinical Follow-Up Study Protocol for PROFEMUR® L Revision Femoral Stems	NCT02314702	MicroPort Orthopedics Inc.	user2@example.com	None	2015-09-04	2027-10-31	2028-10-31	-	-	2025-07-14

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My Organizations' Clinical Trials

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