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Comparison of conventional hand therapy and assistive device in the rehabilitation of flexor tendon injuries

A randomized control trial comparing the functional outcomes in patients with post tendon repair mobilized by conventional hand therapy versus assistive device

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/016821
Enrollment
120
Registered
2019-01-01
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M663- Spontaneous rupture of flexor tendons

Interventions

Intervention1: Mobilization: Assistive device Intervention will be provided for a period of 3 months and 2 sessions daily one in the morning and one in the evening each session will be for a period of

Sponsors

Department of Orthopaedics
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: -Patients with zone II to zone V flexor tendon injuries who have been operated by early primary tendon repair

Exclusion criteria

Exclusion criteria: -Patients with associated fractures, nerve and vascular injury along with tendon injuries of the hand which may affect the rehabilitation. -Patients with tendon injuries of hand with different zones in the same hand -Patients with combined flexor and extensor tendon injuries of hand.

Design outcomes

Primary

MeasureTime frame
Total active flexion and Total active motion (Strictland criteria and Tang criteria)Timepoint: Post operatively at the time of discharge, 3 weeks, 6 weeks, 3 months, 6 months, 12 months

Secondary

MeasureTime frame
Grip strength and pinch strengthTimepoint: At 6 months and 12 months post intervention;Quick dash scoreTimepoint: Postop at the time of discharge, 3 weeks, 6 weeks, 3 months, 6 months, 12 months post intervention

Countries

India

Contacts

Public ContactVenkata Vinay Atluri

Kasturba Medical college Manipal

anmacharya@gmail.com8217736961

Outcome results

None listed

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