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A Randomized Controlled Trial of Different Methods in Repairing Acute Rupture of Flexor Tendon in Hand

A Randomized Controlled Trial of Different Methods in Repairing Acute Rupture of Flexor Tendon in Hand

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17011694
Enrollment
Unknown
Registered
2017-06-19
Start date
2017-07-01
Completion date
Unknown
Last updated
2017-07-03

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

Conditions

acute rupture of flexor digitorum tendon in hand

Interventions

Group A:2-0 braided polyester suture was used. The modified Kessler method was used to match the tendon. After the anastomosis, the outer membrane of the tendon was repaired by 4-0 braided polyester t
Group B:Application of 2-0 braided polyester suture, using modified Kessler method to match the tendon

Sponsors

Shanghai Jiaotong University Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) Those whose flexor digitorum tendon (from the insertion of the superficial flexor tendonin to the insertion of the flexor digitorum tendon nearly 1cm) in hand was ruptured completely (within 8 hours from the injury); 2) Those whose ruptured tendon can be repaired by phase I after the assessment by the surgeon; 3) Those whose ruptured tendon can be repaired by Kessler suture anastomosis after the assessment by the surgeon; 4) Aged 20 to 60 years old, male and female; 5) Those who have informed consent and signed informed consent before surgery.

Exclusion criteria

Exclusion criteria: 1) history of tendon injury or traumatic brain injury; 2) combined extensor tendon injury or tendon injury involving multiple fingers; 3) associated with upper limb fractures, blood vessels, nerve injury; 4) history of malignant tumors; 5) associated with skin defects; 6) accompanied by mental illness history, dementia, etc. can not be normal, accurate communication and answer questions; 7) physically handicapped; incapacitated; 8) do not want or can not cooperate with the data collector; 9) maternal and other incompatible persons.

Design outcomes

Primary

MeasureTime frame
Metacarpophalangeal joint activity;Proximal interphalangeal joint activity;Distal interphalangeal joint activity;

Secondary

MeasureTime frame
VAS score;DASH sore;MHQ score;Ipsilateral hand relative grip strength (compared with the contralateral);the repaired tendon has ruptured again or not;Whether it is necessary to re-release surgery;

Countries

China

Contacts

Public ContactXianyou Zheng

Shanghai Jiaotong University Affiliated Sixth People's Hospital

zhengxianyou@126.com+86 13916180968

Outcome results

None listed

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