Last reviewed · How we verify

NCT06866899

Axillary Block or Wide-awake Local Anesthesia for Complex Regional Pain Syndrome (CRPS) Following Common Hand Surgeries

Completed Last updated 10 March 2025
What this trial tests

trial testing Surgery for Dupuytren contracture (DC), DeQuervain tenosynovitis (DQS), carpal tunnel syndrome (CTS), or trigger finger (TF) in CRPS in 98 participants. Completed in 1 July 2024.

Timeline
1 January 2021
Primary endpoint
1 June 2024
1 July 2024

Quick facts

Lead sponsorAnkara University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment98
Start date1 January 2021
Primary completion1 June 2024
Estimated completion1 July 2024
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Ankara University

Who can join

18 and older, any sex, with CRPS or Walant. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Flare reaction, characterized by excessive erythema, stiffness, and edema postoperatively, can lead to complex regional pain syndrome (CRPS) when pain is present. This study compares flare and CRPS incidence following hand surgeries performed under regional anesthesia with axillary block (RAAB) and WALANT (Wide-Awake Local Anesthesia No Tourniquet).

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 recruiting trials for CRPS

Currently open trials in the same condition.

Other Ankara University 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/NCT06866899.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing