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Comparison between efficacy of combination of drugs with additives given for spinal anaesthesia.

Comparison between Efficacy of Intrathecal Tramadol-Bupivacaine(H) and Fentanyl- Bupivacaine(H) in lower abdominal surgeries â?? a one year hospital based randomized control trial conducted at KLEs Dr. PRABHAKAR KORE charitable hospital and research centre, Belagavi.â??

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/05/033466
Enrollment
100
Registered
2021-05-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: L089- Local infection of the skin and subcutaneous tissue, unspecified Health Condition 2: O- Medical and Surgical Health Condition 3: M958- Other specified acquired deformities of musculoskeletal system Health Condition 4: S729- Unspecified fracture of femur Health Condition 5: S899- Unspecified injury of lower leg Health Condition 6: N23- Unspecified renal colic

Interventions

Intervention1: Fentanyl: Adding either fentanyl 25 micrograms or tramadol 25 mg along with 3 cc of 0.5%bupivacaine in intrathecal injection to increase the duration of the block. Control Intervention1

Sponsors

Dr Prabhakar Kore hospital and medical research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing elective lower abdominal surgery falling under ASA Grade 1 or 2, weighing between 50 to 70 kgs and height between 150 to 175 Cms

Exclusion criteria

Exclusion criteria: Hypovolemic patients, spinal deformity, uncooperative patients, contraindications to spinal anaesthesia, pregnant patients, pre existing neurologic deficits and those not willing to be part of trial.

Design outcomes

Primary

MeasureTime frame
Time taken to achieve sensory blockade and motor blockade using modified bromage score. And duration of sensory and motor blockade.Timepoint: From the time of giving spinal anaesthesia to 10 minutes duration and post surgery 3 hour duration to record duration of block.—

Secondary

MeasureTime frame
Level of Sedation using modified Wilson score and bradycardia.Timepoint: From modified Wilson scale 1 to 4 and bradycardia seen during surgery.—

Countries

India

Contacts

Public ContactMohammed Tabrez Khan

JawaharLal nehru medical college, Dr Prabhakar Kore hospital and medical research centre.

profsanikop@gmail.com9448863688

Outcome results

None listed

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