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Ketorolac Versus Triamcinolone Acetonide Injection for the Treatment of de Quervian’s Tenosynovitis: A Double-Blind Randomized Controlled Trial

Ketorolac Versus Triamcinolone Acetonide Injection for the Treatment of de Quervian’s Tenosynovitis: A Double-Blind Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200909006
Enrollment
78
Registered
2020-09-09
Start date
2020-10-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

de Quervian’s Tenosynovitis De Quervain’s tenosynovitis&#44

Interventions

1 mL ketorolac 30 mg/mL + 0.5 mL 1% lidocaine with adrenaline,1 ml triamcinolonacetonide 10 mg/ml + 0.5 mL 1% xylocaine with adrenaline
Experimental Drug,Active Comparator Drug
Ketorolac injection,Triamcinolone Acetonide Injection

Sponsors

None
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 20 years old 2. The patients will require to have all of the following two physical findings: 2.1 Radial styloid tenderness 2.2 Pain at the radial wrist with resisted extension or abduction of the thumb 2.3 Positive Finkelstein’s test or WHAT test.

Exclusion criteria

Exclusion criteria: 1 Patients who allergy to NSAIDs or same group of ketorolac (e.g. diclofenac) 2 History of severe complication from corticosteroid injection or ketololac injection including anaphylaxis 3 Prior treatment in the last six months with steroid injection and/or surgery at the same anatomical location. 4 Possible traumatic or neoplastic origin of symptoms 5 Patient had inflammatory joint disease at the affected wrist. 6 Inability to fill in follow-up forms or absence of self determination in the participant patient. 7 Patients with pre-existing condition with high risk of drug AE (e.g. ketorolac related to platelet dysfunction) 8 Patient who participate another research in the same time of this project

Design outcomes

Primary

MeasureTime frame
Treatment successfull at the 6 weeks post injection all three physical signs will completely resolve resolve and the patient has at least 90% improvemen

Secondary

MeasureTime frame
Pain score before injection date and at the 6 weeks post injection a visual numerical rating scale, with 0 indicating no pain and 10 indicating extremely intense pain

Contacts

Public ContactSITTHIPHONG SUWANNAPHISIT

Faculty of Medicine, Prince of Songkla University,

aunsittipong@gmail.com+66909829595

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026