Trials / Completed
CompletedNCT03067194
The Study to Evaluate Efficacy and Safety of Celecoxib Capsule in Hand Osteoarthritis Patients
Open-label, Multicenter, Randomized Study to Assess the Efficacy and Safety of Celecoxib 200mg Capsule QD and Celecoxib 100mg BID in Hand Osteoarthritis Patients
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 117 (actual)
- Sponsor
- Chong Kun Dang Pharmaceutical · Industry
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate efficacy and safety of Celecoxib capsule in hand osteoarthritis patients.
Detailed description
This is a six-weeks, open-label, multi-center, randomized study. Patients take Celecoxib 200mg capsule once a day or Celecoxib 100mg capsules twice per day. If patients do not tolerate the pain, they are able to take Acetaminophen as a rescue medication during 6 weeks.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Celecoxib 100 MG | Celecoxib 100mg, Oral, BID(twice per day), During 6 weeks |
| DRUG | Celecoxib 200mg | Celecoxib 200mg, Oral, QD(once daily), During 6 weeks |
Timeline
- Start date
- 2016-12-27
- Primary completion
- 2017-07-10
- Completion
- 2018-11-20
- First posted
- 2017-03-01
- Last updated
- 2020-01-30
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03067194. Inclusion in this directory is not an endorsement.