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Comparison of two heavy bupivacaine in patients undegoing surgery below umbilicus under spinal anaesthsia

Comparison of hyperbaric bupivacaine versus hyperbaric levobupivacaine in subarachnoid block for infra umbilical surgery: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049812
Enrollment
60
Registered
2023-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Hyperbaric bupivacaine: Single injection of hyperbaric bupivacaine 15mg in the subarachnoid space producing subarachnoid block with duration of 2.5 hours Intervention2: Hyperbaric lev

Sponsors

Department of Anaesthesia and Intensive Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anaesthesiologists (ASA) physical status I and II of either sex BMI >= 20 to Duration of surgery 2- 2.5 hours in infraumbilical surgeries (Inguinal hernias, Transurethral resection of prostate, Gynaecological surgeries).

Exclusion criteria

Exclusion criteria: Pre-existing local infection at the site of subarachnoid block Patients with coagulopathy and platelet disorders. Contraindication or allergy to study drugs Patients having pain in any other area than the surgery site Patients having sensory or motor problem in the lower limb Patients who failed to understand the VAS scoring system Pregnant and lactating women Patients with current history of psychiatric illness, communication difficulties

Design outcomes

Primary

MeasureTime frame
Comparison of duration of motor block after injecting the drugs intrathecallyTimepoint: Assessment of sensory block will be done using sterile pin prick method and motor block will be assessed using Modified Bromage scale. Sensory and motor blockade will be assessed every minute for the first 10 minutes and thereafter every 10 mins during surgery and every 15 minutes postoperatively.

Secondary

MeasureTime frame
Comparison of onset of sensory and motor block, peak level, time to 2 segment regression, duration of effective analgesia and any side effects of drug or procedureTimepoint: 4,8,12,24 hours postoperatively

Countries

India

Contacts

Public ContactDr Jasveer Singh

Government Medical College and Hospital

drjassy18@gmail.com9646121664

Outcome results

None listed

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