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comparison of post-operative pain during 2 weeks after rotator cuff repair surgery between patients received interscalene block alone and patients received interscalene block and intravenous morphin

comparison of post-operative pain during 2 weeks after rotator cuff repair surgery between patients received interscalene block alone and patients received interscalene block and intravenous morphin

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210415050976N13
Enrollment
120
Registered
2023-12-29
Start date
2024-01-08
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

rotator cuff repair. Rotator cuff tear or rupture, not specified as traumatic

Interventions

Intervention 1: Intervention group1: They will be subjected to intrascalene block with 30 ml of half percent ropivacaine before surgery. Intervention 2: Intervention group2: In addition to the intersc

Sponsors

Jahrom University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Candidate patients for open shoulder cuff repair surgery Patients with class (ASA) I, II

Exclusion criteria

Exclusion criteria: Patients with drug sensitivity to the drugs used in the study Liver and kidney problems Hormonal problems Patients with a history of chemotherapy and radiotherapy Having acute or chronic accompanying pain alcohol consumption Corticosteroid use drug addiction Benzodiazepine receptors pregnancy Types of neuropathy such as diabetes

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: In recovery, 6 hours, 12 hours, 24 hours, 48 hours, one week, ten days and two weeks after the operation. Method of measurement: Numerical pain rating scale.

Secondary

MeasureTime frame
The total amount of morphine consumed. Timepoint: in recovery. Method of measurement: mg injected into the patient.;The total amount of pethidine consumed. Timepoint: In Ward. Method of measurement: mg injected into the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNavid Kalani

Jahrom University of Medical Sciences

k.navid@jums.ac.ir+98 71 5434 4002

Outcome results

None listed

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