Ankylosis clinical trials
The registry lists 83 studies for Ankylosis across more than 10 countries. 18 are recruiting or about to start. 37 of them are mainly about Ankylosis (how this is decided). Per ClinicalTrials.gov, last updated 2026-11-03. Counting its 3 narrower conditions too, such as Spondylitis, Ankylosing: 751 studies, 158 open.
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Who runs them
MicroPort Orthopedics Inc. (12) · Paragon 28 (2) · SPINEVISION SAS (2) · Stryker Trauma and Extremities (2) · Assistance Publique - Hôpitaux de Paris (2) · Integra LifeSciences Services (2) · University Hospital, Strasbourg, France (2) · Oslo University Hospital (2)
What is being tested here
Drugs under test in Ankylosis studies, those with the most open studies first. Medicines only given beside them are not counted. How drugs are counted
Coming up
Studies recruiting or running, from their records. “Main data collection” ends at the primary completion date, the sponsor’s own estimate, which often moves.
All 8
- Dec 2026Return to Cross Country Skiing and Other Physical Activities After Arthrodesis of the First Metatarsophalangeal Joint · Oslo University Hospital
- Dec 2026Effectiveness of Retrolaminar Block in Lumbar Spine Fusion With Multimodal Analgesia · Pontificia Universidad Catolica de Chile
- Jun 2027Post Market Follow-Up Study of the EVOLUTION® Total Knee Arthroplasty System With Cruciate Sacrificing Inserts · MicroPort Orthopedics Inc.
- Jun 2027PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular Components · MicroPort Orthopedics Inc.
- Jun 2027Virtual Planning of Total Temporomandibular Joint Replacement · Lund University Hospital
- Jul 2027Safety and Performance of the SPINEVISION Hexanium ACIF in the Treatment of Cervical Spine Degenerative Disc Disease · SPINEVISION SAS
- Oct 2027Safety and Performance of the Hexanium TLIF System in the Treatment of Degenerative Disc Disease · SPINEVISION SAS
- Nov 2027Post Market Clinical Follow-Up Study Protocol for PROFEMUR® TL Modular Femoral Stems · MicroPort Orthopedics Inc.
Who these studies take
Of the 13 Ankylosis studies recruiting now, 10 (77%) set no upper age limit and 3 (23%) stop at 75 or younger. 3 (23%) take children under 18. 0 (0%) are for women only and 0 (0%) for men only; 4 (31%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 2 (15%) | 2 (15%) |
| 18 | 12 (92%) | 12 (92%) |
| 30 | 11 (85%) | 11 (85%) |
| 40 | 12 (92%) | 12 (92%) |
| 50 | 12 (92%) | 12 (92%) |
| 65 | 12 (92%) | 12 (92%) |
| 75 | 12 (92%) | 12 (92%) |
| 85 | 10 (77%) | 10 (77%) |
Across all 83 studies, recruiting or not: 22% stop at 75 or younger and 11% at 65; 13% take children; 0% are for women only and 0% for men only; 14% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
How long Ankylosis studies take
Of 20 interventional studies with no phase under Ankylosis, half reached primary completion within 53 months of starting, counting those still running.
| Start to primary completion | Every sponsor | Industry | Non-industry |
|---|---|---|---|
| Interventional, no phase | 53 mo32–59 · 20 studies | — | — |
Each figure is the month by which half the studies had reached primary completion, with the range in which the middle half did. Studies still running count until their last registry update; studies that stopped early are left out. Phase 1 includes early phase 1; observational means prospective or not stated, as retrospective and cross-sectional studies date a window of data rather than a study. How these figures are worked out
What changed recently
From the registry's own updates since Oct 13, 2026.
Newly registered1
Studies
Recruiting first, then most recently updated. Showing 50 of 83. Browse all 83 → or search them.
- Alloplastic Total Temporomandibular Joint (TMJ) Replacement RegistryRecruitingNCT0399172815 countries
- Evaluation of the Effect of Reiki on Pain After Lumbar SurgeryRecruitingNCT07722117Not applicable1 country
- Clinical Outcomes Study of the Nexel Total ElbowRecruitingNCT02469662Not applicable8 countries
- Effectiveness of Retrolaminar Block in Lumbar Spine Fusion With Multimodal AnalgesiaRecruitingNCT07291388Not applicable1 country
- Return to Cross Country Skiing and Other Physical Activities After Arthrodesis of the First Metatarsophalangeal JointNot yet recruitingNCT07610330
- Safety and Performance of the Hexanium TLIF System in the Treatment of Degenerative Disc DiseaseRecruitingNCT059971212 countries
- Performance and Safety Evaluation of Inion CompressOn Screw in Foot and Ankle Surgeries. PMCF InvestigationRecruitingNCT05555459Not applicable1 country
- Virtual Planning of Total Temporomandibular Joint ReplacementRecruitingNCT073731841 country
- Clinical, Microbial and Tissue-based Characterization of Patients Treated for Severe Temporomandibular Joint PathologyNot yet recruitingNCT07350239
- Evaluation of the Efficacy and Safety of Absorbable vs Traditional Bone Wax for Facet Fusion After Lumbar Fusion SurgeryNot yet recruitingNCT07040293Not applicable1 country
- Registry of Arthrex Hand and Wrist ProductsRecruitingNCT050466001 country
- Wrist and Carpal Arthrodeses. A 1-year Follow-up Study.RecruitingNCT069172351 country
- Efficacy and Tolerance Study of B-DYN Versus Conventional Fusion in the Treatment of Lumbar Stenosis on the Degree of Post-operative Functional Incapacity (BDYNCLIN)RecruitingNCT04407338Not applicable1 country
- Post Market Clinical Follow-Up Study for PROFEMUR® Preserve Classic Femoral StemEnrolling by invitationNCT041475591 country
- Prospective SPINE RegistryRecruitingNCT041765623 countries
- Instrumented POsterolateral Arthrodesis for Adolescent Idiopathic ScoliosisRecruitingNCT051457251 country
- Post Market Clinical Follow-Up Study Protocol for PROCOTYL® C Acetabular ComponentsEnrolling by invitationNCT035765731 country
- Ketorolac vs Oxycodone for Great Toe ArthrodesisRecruitingNCT05054868Phase 11 country
- Subtalar & Talonavicular Arthrodesis v.s Subtalar & Naviculocuniform Arthrodesis for Progressive Collapsing Foot DeformityCompletedNCT07878000Not applicable1 country
- Ultrasound-Guided Percutaneous Peripheral Nerve Stimulation: A Department of Defense Funded Pragmatic Clinical TrialCompletedNCT04713098Not applicable1 country
- Foot and Ankle Arthrodesis or Osteotomy With Io-Fix Type FixationCompletedNCT04812353Not applicable1 country
- Lumbar Fusion With Porous Versus Non-Porous CagesActive, not recruitingNCT05583864Not applicable1 country
- Efficacy and Safety Study of Lumbar Interbody Fusion With MatriTMBONE Associated With Autologous Bone MarrowTerminatedNCT01335243Phase 21 country
- Collecting Bone Graft During Spinal Decompression and Posterolateral Lumbar Fusion to Better Define Bone Making CellsActive, not recruitingNCT014099541 country
- Early Weight-Bearing After the Lapiplasty ProcedureActive, not recruitingNCT03740282Not applicable1 country
- Safety and Performance of the SPINEVISION Hexanium ACIF in the Treatment of Cervical Spine Degenerative Disc DiseaseActive, not recruitingNCT061554091 country
- Treatment Outcomes for Ankle ArthritisCompletedNCT003913651 country
- ViviGen Cellular Bone Matrix for Hindfoot or Ankle ArthrodesisCompletedNCT041380171 country
- Impact of Pelvic Joint Stiffness on the Fear of Falling in Subjects Aged Over 75 YearsCompletedNCT070237181 country
- The SpeedPlate™ Rapid Compression Implant Study (The SPRINT™ Study)Active, not recruitingNCT065485811 country
- Compression Nail for Tibiocalcaneal ArthrodesisCompletedNCT037804521 country
- Comparison of Ultrasonic Osteotome and Conventional Drill OsteotomeCompletedNCT02487901Not applicable1 country
- Wright Foot & Ankle Post-Market Observational StudyTerminatedNCT041188944 countries
- Effect of Osteopathy Medicine on Post-surgical Management of Lumbosacral ArthrodesisCompletedNCT06669858Phase 21 country
- Efficacy of First MTPJ Arthrodesis as a Treatment in Hallux RigidusActive, not recruitingNCT04590313Not applicable1 country
- Vanguard Rocc Post Market SurveillanceActive, not recruitingNCT036647914 countries
- 3rd-year Post-surgical Evaluation of Adjacent Segment Disc Degeneration Onset in Lumbar Spine (Spinal Fusion vs. Lumbar Arthroplasty With Disc Replacement)WithdrawnNCT055613221 country
- Retrospective Evaluation of Clinical and Radiographic Outcomes Following Total Talus ReplacementCompletedNCT052313041 country
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator HA Coated Modular Femoral StemsTerminatedNCT023146111 country
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® TL Modular Femoral StemsActive, not recruitingNCT022397831 country
- Low-dose Dual-energy CT for the Pre-surgical Planning of Patients With Progression of ScoliosisCompletedNCT034838441 country
- Post Market Clinical Follow-Up Study Protocol for CONSERVE® Press-Fit Femoral ComponentsActive, not recruitingNCT022858421 country
- Post Market Clinical Follow-up Study Protocol for DYNASTY® BioFoam® Acetabular ComponentsActive, not recruitingNCT021496671 country
- Study of the Effects of Hypnosis Before Undergoing Surgery, on Anxiety in Children Aged 10 to 18 YearsCompletedNCT01320956Not applicable1 country
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® Gladiator Cemented Femoral StemsTerminatedNCT02397746
- Post Market Clinical Follow-Up Study Protocol for PROFEMUR® L Revision Femoral StemsActive, not recruitingNCT023147021 country
- Post Market Follow-Up Study of the EVOLUTION® Total Knee Arthroplasty System With Cruciate Sacrificing InsertsActive, not recruitingNCT023514145 countries
- Multi-Plane Hallux Valgus Correction With the Phantom® NailCompletedNCT040842621 country
- Percutaneous Trans-facet Screw Fixation Under CT-scan Guidance for Remaining Symptoms at a Distance of Previous Spinal SurgeryCompletedNCT055250521 country
- PMCF Study Protocol for PROFEMUR® Gladiator Plasma Femoral Stems and PROCOTYL® L Beaded Acetabular ComponentsActive, not recruitingNCT028238341 country