Skip to content

A randomized control trial to evaluate the effect of addition of intrathecal clonidine to hyperbaric bupivacaine on postoperative pain after lower segment caesarean section

A randomized control trial to evaluate the effect of addition of intrathecal clonidine to hyperbaric bupivacaine on postoperative pain after lower segment caesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2012/09/002946
Enrollment
105
Registered
2012-09-03
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 parturients

Interventions

Intervention1: clonidine: 50mcg clonidine or 75mcg clonidine are used intrathecally with hyperbaric bupivacaine and duration of postoperative analgesia compared Control Intervention1: fentanyl: 25mcg

Sponsors

Lady Hardinge Medical College Associated Shrimati Sucheta Kriplani Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 105 healthy parturients (ASA physical status I and II) carrying a singleton fetus at term, scheduled to undergo elective lower segment caesarean section under spinal anaesthesia

Exclusion criteria

Exclusion criteria: who refused spinal anaesthesia, had any contraindication to regional anaesthesia, had fetal distress, preterm gestation, hypertensive disorders of pregnancy, multiple pregnancy, weighed more than 90 kg, were less than 140 cm or more than 170 cm in height, had any major co-morbidity or if they were unable to communicate in either english or hindi language

Design outcomes

Primary

MeasureTime frame
Duration of postoperative analgesiaTimepoint: the time from intrathecal injection of the drug to the time when patient first requests analgesia in the postoperative period

Secondary

MeasureTime frame
Heart rate, Systolic Blood Pressure, Diastolic Blood Pressure, Mean Arterial Blood Pressure,Onset and duration of sensory block and motor blockade, Level of sedation, Quality of surgical anaesthesia, Supplemental drug and vasopressor requirement, Side effects, Umbilical artery blood gas analysis and neonatal Apgar scoreTimepoint: Time from giving spinal to time when Hollmen scale 3 was achieved at T6 level as onset of sensory block Time from giving spinal to time Bromage scale 4 was achieved as onset of motor block Apgar at 1 min and at 5 min Maternal sedation every 15 min Duration of sensory block as time from IT injection to time till regression below T12 Duration of motor blockade as time from IT injection to time till Bromage scale reaches 1

Countries

India

Contacts

Public Contactranju singh
mamcdeepti@gmail.com

Outcome results

None listed

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