Treatment of the Distal Radius Fracture with Closed Reduction and Percutaneous Pinning without ?Superficial Radial Nerve Exploration

Comparison of the Treatment of the Distal Radius Fracture with Closed Reduction and Percutaneous Pinning with and without ?Superficial Radial Nerve Exploration

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190903044677N1

Enrollment

100

Registered

2019-11-09

Start date

2019-11-22

Completion date

Unknown

Last updated

2019-12-17

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

Conditions

Distal radius fracture. Stress fracture, right radius, initial encounter for fracture

Interventions

Intervention 1: Intervention group: Treatment of distal radius fracture with closed reduction and percutaneous pinning without ?superficial radial nerve exploration. Intervention 2: Control group: Tre

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age of more than 18 years Providing written consent to participate in the study

Exclusion criteria

Exclusion criteria: A history of distal radius fracture Concomitant injury affecting the outcome of treatment

Design outcomes

Primary

Measure	Time frame
First dorsal web sensation. Timepoint: Before the intervention and two days after the end of intervention. Method of measurement: Patients' clinical examination.;Paresthesia?. Timepoint: Before the intervention and two days after the end of intervention. Method of measurement: Patients' clinical examination.;Hyperesthesia?. Timepoint: Before the intervention and two days after the end of intervention. Method of measurement: Patients' clinical examination.	—

Measure

Time frame

First dorsal web sensation. Timepoint: Before the intervention and two days after the end of intervention. Method of measurement: Patients' clinical examination.;Paresthesia?. Timepoint: Before the intervention and two days after the end of intervention. Method of measurement: Patients' clinical examination.;Hyperesthesia?. Timepoint: Before the intervention and two days after the end of intervention. Method of measurement: Patients' clinical examination.

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Secondary

Measure	Time frame
Wrist range of motion. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: Goniometer.;Wrist function. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: DASH questionaire.;Pinch strength. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: Dinamometer.;Pain. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: Visual analogue scale.	—

Measure

Time frame

Wrist range of motion. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: Goniometer.;Wrist function. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: DASH questionaire.;Pinch strength. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: Dinamometer.;Pain. Timepoint: Before the intervention and 12 months after the end of intervention. Method of measurement: Visual analogue scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactPouria Tabrizian

Shafa Orthopedic Hospital

tabrizian.p@iums.ac.ir+98 21 3354 2041

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026