Comparison of mean arterial blood pressure and heart rate using a local anesthetic dose based on height and weight versus height alone for caesarean section.

Comparison of hemodynamics using levobupivacaine dosage based on height and weight versus height alone for elective caesarean section under subarachnoid block. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/12/078703

Enrollment

Registered

2024-12-27

Start date

Unknown

Completion date

Unknown

Last updated

2025-02-03

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

Conditions

Health Condition 1: O994- Diseases of the circulatory systemcomplicating pregnancy, childbirth and the puerperium Health Condition 2: O94- Sequelae of complication of pregnancy, childbirth, and the puerperium

Interventions

Intervention1: To compare the mean arterial pressure using isobaric levobupivacaine dosage based on height and weight vs height alone for elective caesarean section under subarachnoid block.: To comp

Eligibility

Inclusion criteria

Inclusion criteria: Parturients of age 18yr to 35yr with ASA grade 2 with weight of 50kg to 100kg and height of 140 cm to 180cm undergoing elective caesarean section with singleton pregnancy will be included.

Exclusion criteria

Exclusion criteria: 1. Allergy to local anaesthetic. 2. Contraindication to spinal anaesthesia (for e.g.- coagulopathy, spine deformity, local site infection)

Design outcomes

Primary

Measure	Time frame
To compare the mean arterial pressure using isobaric levobupivacaine dosage based on height & weight versus height alone for elective caesarean section under subarachnoid block.Timepoint: Baseline 2 min 4 min 6 min 8 min 10 min 12 min 14 min 15 min 20 min 25 min 30 min 35 min 40 min 45 min 50 min	—

Secondary

Measure	Time frame
To compare - Effect on spinal block characteristics in both the groups.Timepoint: Time to achieve T6 sensory block (in minutes) Maximum sensory block after 20 minutes (in minutes) Time of two segment regression Time to achieve Bromage score 3 Time of first analgesic requirement in post operative period. Time of surgery;To compare -1. The incidence of adverse events like nausea, vomiting, shivering & headache. 2. Neonatal outcome in both the groups.Timepoint: Time of oxytocin infusion (in minutes) APGAR score at 1 minute APGAR score at 5 minutes	—

Measure

Time frame

To compare - Effect on spinal block characteristics in both the groups.Timepoint: Time to achieve T6 sensory block (in minutes) Maximum sensory block after 20 minutes (in minutes) Time of two segment regression Time to achieve Bromage score 3 Time of first analgesic requirement in post operative period. Time of surgery;To compare -1. The incidence of adverse events like nausea, vomiting, shivering & headache. 2. Neonatal outcome in both the groups.Timepoint: Time of oxytocin infusion (in minutes) APGAR score at 1 minute APGAR score at 5 minutes

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Countries

India

Contacts

Public ContactDr Rajesh Sood

ESIC Medical College and Hospital, Faridabad.

drsoodrajesh@gmail.com9810218916

Outcome results

None listed

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