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Investigating the effect of curcumin tablets on pain, blood pressure and blood coagulation in patients undergoing surgery for benign prostatic hyperplasia through urethral incisio

Phase 4
Recruiting
Conditions
Hyperplasia of prostate.
Enlarged prostate
Registration Number
IRCT20231022059810N1
Lead Sponsor
Ghoum University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
184
Inclusion Criteria

Patients who have undergone prostate urethral resection surgery
Not having coagulation disorders
Not having an allergy to curcumin
Not having drug addiction

Exclusion Criteria

Abnormal bleeding after surgery (more than 300 cc)
Criticality of the patient's vital signs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Immediately before the intervention and every 6 hours after the intervention until discharge. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: Immediately before the intervention and every 6 hours after the intervention until discharge. Method of measurement: Vital Sign Monitoring Device.;Blood coagulation tests. Timepoint: Immediately before the intervention and every 24 hours after the intervention until discharge. Method of measurement: Using PT, PTT, INR laboratory tests.
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