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Investigating the effect of hemostasis on the surgical treatment of rotator cuff tears

Investigating the effect of hemostasis after arthroscopic repair of rotator cuff tear on pain and movement limitation of patients after surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240707062352N2
Enrollment
60
Registered
2025-03-06
Start date
2025-05-31
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Repair of rotator cuff tear, limitation of movement after surgery, pain after surgery. Injury of muscle(s) and tendon(s) of the rotator cuff of shoulder

Interventions

Intervention 1: Intervention group: The patients blood pressure is measured in the ward and pre-op and its average is recorded as the patients pre-operative pressure. Then after debridement and before

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 70 Years

Inclusion criteria

Inclusion criteria: Repairable rotator cuff tear between 15 and 70 years old

Exclusion criteria

Exclusion criteria: Irreparable rotator cuff tear History of infection Revision surgery Acute traumatic rotator cuff tear in the last 3 months The presence of other simultaneous pathologies in the shoulder History of coagulopathy and use of anticoagulant drugs History of liver and kidney diseases Drug use

Design outcomes

Primary

MeasureTime frame
Shoulder passive movements. Timepoint: Before surgery, 4, 6 and 12 weeks after surgery. Method of measurement: in degrees and by goniometer.

Secondary

MeasureTime frame
The pain. Timepoint: Before surgery and 2, 4, 6, 12 weeks after surgery. Method of measurement: VAS scale.;Taking oxycodone tablets. Timepoint: 2 weeks after surgery. Method of measurement: Number of pills taken.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Ghoraishian

Islamic Azad University

M.ghoraishian@gmail.com+98 21 4486 7262

Outcome results

None listed

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