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Comparison of pain after abdominal surgery in patients receiving Nasocalcin spray or vitamin D and Nasocalcin spray

Phase 2
Conditions
Pain after abdominal surgery.
Unspecified complication of procedure
T81.9
Registration Number
IRCT20230110057093N1
Lead Sponsor
Islamic Azad University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
34
Inclusion Criteria

Having an age between 15-75 years
Signing a personal and informed consent form to participate in the study
1?2ASA
No abuse of drugs and alcohol
Elective surgery

Exclusion Criteria

Loss of consciousness
Hemodynamic disorder
Abnormal intraoperative bleeding
length of the operation more than 4 hours

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: In recovery and at 6, 12, 24 hours after the operation, the amount. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
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