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Comparative study of outcome of closed suction drainage with non-use closed suction drainage in patients with operative treatment of distal end radius fracture

Comparative study of outcome of closed suction drainage with non-use closed suction drainage in patients with operative treatment of distal end radius fracture

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250107004
Enrollment
28
Registered
2025-01-07
Start date
2018-04-04
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

Distal end radius fracture treating with surgical management. Distal end radius, drain placement, pain score, complication

Interventions

After surgery, the participants will place with radivac drain.,After surgery, the participants will not place the radivac drain.
Experimental Device,No Intervention No treatment
Closed suction drainage,Non-suctional drainage

Sponsors

faculty of medicine, Navamindradhiraj University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with a distal radius fracture who have indications for surgery, such as open distal radius fractures or distal radius fractures that have failed non-surgical treatment. 2. Aged 18-80 years. 3. No history of previous fractures in this area. 4. No history of multiple trauma. 5. No underlying diseases in the reactive inflammation group, including Rheumatoid Arthritis, Systemic Lupus Erythematosus (SLE), or gout. 6. No other risk factors affecting the studied arm. 7. No history of allergy to materials used in the fixation apparatus. 8. Willing to participate in the research.

Exclusion criteria

Exclusion criteria: 1. Patients diagnosed with a distal radius fracture for more than 3 weeks. 2. Smokers. 3. Drink alcohol.

Design outcomes

Primary

MeasureTime frame
wrist circumferential Pre-operative, post-operative 48 hours, post-operative 2 weeks length of wrist circumference

Secondary

MeasureTime frame
Mayo wrist score Pre-operative, post-operative 48 hours, post-operative 2 weeks questionaire

Countries

Thailand

Contacts

Public ContactSitthiphong Suwannaphisit

Navamindradhiraj University

sitthiphong.suw@nmu.ac.th0909829595

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026