FindTrial
Sign In

A clinical trial to compare post operative urinary retention in two drugs bupivacaine and ropivacaine in spinal anaesthesia in patients undergoing hernia surgery.

Post operativeurinaray retention after spinal anesthesia in hernia surgery: A prospective comparative double blind study between ropivacaine heavy 0.75% and bupivacaine heavy 0.5%.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052410
Enrollment
60
Registered
2023-05-09
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangrene Health Condition 2: K429- Umbilical hernia without obstruction or gangrene Health Condition 3: K409- Unilateral inguinal hernia, without obstruction or gangrene

Interventions

Intervention1: Inj. Ropivacaine heavy (3.5 ml) 0.75%: In this group, patients will be asked to void urine before procedure and will measure bladder volume with the help of ultrasound then patient will

Sponsors

Dr Hetal N Kanabar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients posted for hernia surgeries under spinal anaesthesia only. 2 Age between 18-60 years. 3. Patients giving written valid consent 4. ASA physical status I, II and III. 5. Duration of surgery less than 2 hr

Exclusion criteria

Exclusion criteria: 1 Patients with renal and liver diseases. 2 Patients with history of renal surgery or prostate surgery. 3 Patient with Benign prostatic hyperplasia. 4 Patient with recent or past history of any psychiatric illness. 5 Patients with bleeding tendencies and coagulopathy.

Design outcomes

Primary

MeasureTime frame
the primary outcome is to compare duration of first spontaneous voiding or need of cathetarisation postoperatively.Timepoint: 2hr ,4 hr, 6 hr , 8 hr and 10 hours—

Secondary

MeasureTime frame
the secondary outcome is to compare time taken for complete ambulation, Bromage score and time for Rhomberg test to be negative.Timepoint: 2hr ,4 hr, 6 hr , 8 hr and 10 hours.—

Countries

India

Contacts

Public ContactDr Hetal Kanabar

GMERS Medical College Junagadh

Kanabarhetal@yahoo.com9909960401

Outcome results

None listed

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