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Study to compare effect of Bupivacaine with Tramadol and Levobupivacaine with Tramadol for pain in below umblical surgeries after operation by epidural catheter.

Comparitive study of Bupivacaine with Tramadol and Levobupivacaine with Tramadol in below umbilical surgeries for post operative epidural analgesia.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/051462
Enrollment
70
Registered
2023-04-11
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Health Condition 1: N809- Endometriosis, unspecified Health Condition 2: C55- Malignant neoplasm of uterus, partunspecified Health Condition 3: M169- Osteoarthritis of hip, unspecified Health Condition 4: M179- Osteoarthritis of knee, unspecified Health Condition 5: M879- Osteonecrosis, unspecified Health Condition 6: D269- Other benign neoplasm of uterus, unspecified Health Condition 7: M163- Unilateral osteoarthritis resulting from hip dysplasia Health Condition 8: S829- Unspecified fracture o

Interventions

Control Intervention1: BUPIVACAINE WITH TRAMADOL: All the patients having VAS SCORE more then 4 post operatively will be divided into 2 groups.Group 1(BT) will receive 2ml 0.5 percent Bupivacaine wit

Sponsors

Peoples University,bhopal,madhya pradesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA GRADE 1& 2 SCHEDULE FOR ELECTIVE IN BELOW UMBILICAL SURGERIES THAT REQUIRE POST OPERATIVE EPIDURAL ANALGESIA. DOSE OF INJ.BUPIVACAINE 3.5ML WITHOUT ADJUVANT. DURATION OF SURGERY 90-120 MINS.

Exclusion criteria

Exclusion criteria: LACK OF PATIENTS CONSENT. AGE 60YRS. ASA GRADE 3 AND MORE. HISTORY OF SERIOUS PULMONARY DISEASE,ISCHEMIC HEART DISEASE,RENAL/HEPATIC DYSFUNCTION,CORONARY ARTERY OR CERVICAL SPINE DISEASE AND PATIENTS WITH ABNORMAL COAGULATION PROFILE. PATIENTS WITH LOCAL SKIN INFECTIONS. PATIENTS WITH HYPERSENSITIVITY TO ANY OF THE DRUGS USED. PREGNANT AND LACTATING MOTHERS.

Design outcomes

Primary

MeasureTime frame
TO COMPARE NUMBER OF EPIDURAL ANALGESIA (top up) required in first 24 hours in both groups.Timepoint: FIRST 24 HOURS AFTER THE SURGERY—

Secondary

MeasureTime frame
TO COMPARE HEMODYNAMIC CHNAGES IN THE POST OPRETIVE PERIOD.Timepoint: FIRST 24 HOURS AFTER THE SURGERY—

Countries

India

Contacts

Public ContactDr Ankit Gupta

PEOPLES COLLEGE OF MEDICAL SCIENCES & RESEARCH CENTRE BHANPUR BHOPAL

drmahimabatra@gmail.com975207418

Outcome results

None listed

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