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Using of short arm splint for immobilization.

A comparison between outcome of immobilization of upper limb soft tissue injuries by a regular size splint and half size splint.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170105031787N1
Enrollment
300
Registered
2017-12-31
Start date
2017-03-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Upper limb soft tissue injuries. Contusion of finger(s) with damage to nail

Interventions

Intervention 1: Half regular size short splint of upper limb in intervention group. Intervention 2: Regular size of short splint of upper limb in control group.
Treatment - Other
Half regular size short splint of upper limb in intervention group
Regular size of short splint of upper limb in control group

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 139 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients, who admitted in the emergency department of “7tir Hospital” in Tehran with a complaint of upper limb trauma and need splinting

Exclusion criteria

Exclusion criteria: Exclusion criteria: Patients under eighteen years old and those that can not be follow up will be rolled out. Patients who had fracture Patients who had dislocation Patients who had laceration needs to repair

Design outcomes

Primary

MeasureTime frame
Swelling. Timepoint: Before intervention; one week after intervention; two weeks after intervention; three weeks after intervention. Method of measurement: Telephone or in-person interviews with patient.;Recovery time. Timepoint: every week from splinting to removal time. Method of measurement: telephone or in-person interviews with patients.;Pain. Timepoint: every week until 3 weeks from splinting. Method of measurement: telephone or in-person interviews with patients according to pain score.;Complication such as compartment syndrome, burning of skin or sore. Timepoint: every week from splinting to removal time. Method of measurement: telephone or in-person interviews with patients.

Countries

Iran (Islamic Republic of)

Contacts

Public Contact?Shahrzad Behjat

Iran University of Medical Sciences

shahrzad_20us@yahoo.com+98 21 6652 5327

Outcome results

None listed

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