Last reviewed · How we verify
NCT02435134: HIRROM
Examination Chair for Hip Internal Rotation Range of Motion Measurement
trial testing no intervention in Limited Hip Mobility in 30 participants. Completed in 25 January 2017.
25 January 2017
Quick facts
| Lead sponsor | Schulthess Klinik |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 30 |
| Start date | 7 October 2015 |
| Primary completion | 25 January 2017 |
| Estimated completion | 25 January 2017 |
| Sites | 1 location across Switzerland |
Drugs / interventions tested
- no intervention
Conditions studied
- Limited Hip Mobility — all drugs for Limited Hip Mobility →
Sponsor
Schulthess Klinik
Who can join
Adults 18 to 40, any sex, with Limited Hip Mobility. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Hip internal rotation range of motion (HIRROM) assessment is performed to assess the mobility of the hip. The assessment is typically done manually (manual testing), which induces large variability in the results between and within testers. An initial version of an examination chair (EC1) was recently developed with the aim to minimize the variability of testing results for HIRROM assessments. A new version of the examination chair (EC2) has been implemented in order to individualize the testing protocol and will be validated in this study.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT02435134
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of no intervention
Trials testing the same drug.
- NCT07480057 — Assessment of Changes in Bone Mineral Metabolism After Liver Transplantation by Bone Mineral Densitometry · recruiting
- NCT07253506 — Turkish Adaptation, Validity, and Reliability Study of the Patient Experience With Treatment and Self-Management Scale i · not yet recruiting
- NCT07253519 — The Relationship Between Mood and Insomnia Severity and Caregiver Burden in Caregivers of Stroke · not yet recruiting
- NCT07194096 — Stress Hyperglycemia Ratio and Postoperative Delirium · not yet recruiting
- NCT07240337 — Botulinum Toxin Applications in Hemiplegic Patients · recruiting
Other Schulthess Klinik trials
Trials by the same sponsor.
- NCT07197593 — Validity and Reliability of Calf Raise Tests in Patients With Achilles Tendon Rupture and Lateral Ankle Sprain · NA · not yet recruiting
- NCT06223737 — Spine Deformity Patients With Optoelectronic Motion Capture · NA · not yet recruiting
- NCT06330129 — Validity and Reliability of Trunk Strength Device · NA · completed
- NCT06612853 — Validation of the Single-item Sleep Quality Scale · recruiting
- NCT06555991 — Translation and Validation of the SIRSI and TSK-SI Into German · NA · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02435134 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Schulthess Klinik
- Last refreshed: 14 February 2017
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02435134.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing