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Comparing Clinical Effect of Levobupivacaine (local anaesthesia) and bupivacaine (local anaesthesia)in Spinal Anaesthesia for cesarean section.

Comparison of isobaric levobupivacaine versus hyperbaric bupivacaine in spinal anesthesia for cesarean section: A prospective unmatched case control study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/10/010209
Enrollment
100
Registered
2017-10-26
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: null- Healthy (no associated medical illness) parturients advised to undergo cesarean section under spinal anesthesia.

Interventions

Intervention1: Spinal anesthesia: intrathecal injection of local anaesthetic Control Intervention1: levobupivacaine 0.5% 2.5 ml (12.5mg): isobaric levobupivacaine without any additive administered int

Sponsors

Pannadhai Zanana Hospital attached to RNT medical college
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA I,II Healthy parturients advised to undergo elective and semi elective cesarean sections for indications 2.previous CS 3.Breech, 4.Cephalopelvic disproportion 5.Pregnancy following infertility treatment, 6.Postdatism, 7.Cord around neck 8.Non-progress of labour

Exclusion criteria

Exclusion criteria: 1.Allergy to amide Local anesthetic 2.Any associated systemic illness having cardiovascular, neurological, renal, pulmonary, autoimmune, psychiatric, end stage liver disease etc.) 3.Any coagulation abnormality. 4.Morbid obesity 5.Short stature. 6.Having fetal anomaly 7.Any contraindication to spinal anaesthesia

Design outcomes

Primary

MeasureTime frame
Success rate ( number of cases in whom surgery could be completed without supplementation ) Timepoint: Outcome of the study will be observed after the end of surgery and patients recover to preoperative condition.

Secondary

MeasureTime frame
(1) Sensory block characteristics ( time to onset , peak sensory level , and duration) (2) Motor block characteristics (time to onset, maximum motor block , and duration) (3) Duration of analgesia (4) Haemodynamic profile (5) Complications (6) Patient & surgeon satisfaction Timepoint: every min till 10 min, at the end of surgery and every 30 min thereafter till complete recovery achieved

Countries

India

Contacts

Public ContactMadhanmohan C

Rabindranath Tagore medical college

drvinaynaithani@yahoo.co.in9829414752

Outcome results

None listed

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