Study of the Effectiveness of Preoperative Gabapentin in the Control of Postoperative Pain in Patients Undergoing Inguinal Hernia under Spinal Anesthesia
Phase 1
- Conditions
- Inguinal hernia
- Registration Number
- RBR-3fv39rm
- Lead Sponsor
- santa casa de misericordia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Data analysis completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Both genders; age between 18 and 60 years; Maximum BMI of 30; scheduled for inguinal hernioplasty at Hospital São José do Avaí.
Exclusion Criteria
Patients with chronic opioid use; patients with chronic pain; history of chemical dependency; or those allergic to any of the medications used in the study; cardiac respiratory renal or hepatic pathology; BMI above 30 kg /m2; relapsed hernias and inguino-scrotal hernias.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expected outcome #1: Reduction of post-operative pain, assessed by visual analog scale. Data was collected from 4 hours after surgery to a period of 30 days.;Outcome found #1: Patients who received gabapentin had lower levels of postoperative pain compared to patients who received placebo
- Secondary Outcome Measures
Name Time Method Expected outcome #2: Reduction in postoperative morphine consumption. Data were collected up to 24 hours and on the thirtieth day after inguinal hernioplasty surgery.;Outcome found #2: Patients who received gabapentin perioperatively consumed less morphine compared to the group who received placebo. Results were seen at 4 hours and 24 hours after inguinal hernioplasty surgery.