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NCT03868995

The Efficacy of Hypertonic Dextrose Injection to Anterior Talofibular Ligament Sprain

Completed NA Last updated 19 September 2024
What this trial tests

NA trial testing Sham injection in Ankle Sprains in 29 participants. Completed in 31 December 2022.

Timeline
1 November 2019
Primary endpoint
1 July 2021
31 December 2022

Quick facts

Lead sponsorTaipei Medical University WanFang Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment29
Start date1 November 2019
Primary completion1 July 2021
Estimated completion31 December 2022
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Taipei Medical University WanFang Hospital

Who can join

Adults 20 to 70, any sex, with Ankle Sprains. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Anterior talofibular ligament is the most injured ligament in ankle sprain. Investigators will include ankle sprain patients who have ankle pain or instability more than 3 months. Ultrasonography will be done for confirm ligament injury. Participants will be randomized into two groups. Participants in dextrose injection group will accept dextrose 15% injection to tendon and enthesis. In the other hand, subcutaneous sham injection to control group. Pain condition, stability test and function test, will be evaluated in 1 week, 4 weeks and 12 weeks after injection.

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:

Other trials of Sham injection

Trials testing the same drug.

Other recruiting trials for Ankle Sprains

Currently open trials in the same condition.

Other Taipei Medical University WanFang Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT03868995.

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