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Comparison of drug modification in Spinal Anesthesia for pregnant women posted for elective cesarean section

A Comparative Evaluation of Intrathecal dexmedetomidine versus Fentanyl as adjuvants to hyperbaric Bupivacaine for cesarean delivery - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/107640
Enrollment
60
Registered
2026-04-06
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: O61- Failed induction of labor Health Condition 2: O63- Long labor Health Condition 3: O64- Obstructed labor due to malposition and malpresentation of fetus Health Condition 4: O65- Obstructed labor due to maternal pelvic abnormality Health Condition 5: O66- Other obstructed labor Health Condition 6: O75- Other complications of labor and delivery, not elsewhere classified Health Condition 7: O76- Abnormality in fetal heart rate and rhythm complicating labor and delivery Healt

Interventions

Intervention1: Adjuvants in Spinal Anesthesia: A randomised control trial of dexmedetomidine and fentanyl as adjuvants in spinal anesthesia foe cesaren section Intervention2: intrathecal administratio

Sponsors

DrSDinesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Parturients aged between 18 to 35 years ASA PS II Singleton pregnancy undergoing elective cesarean section GA more than 37 weeks patients informed and written consent obtained

Exclusion criteria

Exclusion criteria: Refusal for spinal anesthesia contraindications to spinal anesthesia Allergy to study drugs with comorbidities like hypertension diabetes cardiac disease preeclampsia eclampsia multiple pregnany and fetal distress patients on alpha2 agonistor antagonist

Design outcomes

Primary

MeasureTime frame
To compare the Onset and Duration of sensory and motor blockade produced by intrathecal dexmedetomidine and fentanyl when added to hyperbaric bupivacaine in cesarean deliveryTimepoint: The onset of sensory of sensory block will be assessed using a pinprick test every 2 minutes until T6 level is achieved. Hemodynamic parameters like BP, Pulse and SpO2 will be recorded for every 2 minutes in first 10 minutes and every 5 minutes until end of surgery and every 15 minutes in recovery—

Secondary

MeasureTime frame
onset of sensory and motor block duration of motor block duration of analgesia hemodynamic changesTimepoint: maternal an fetal outcomes—

Countries

India

Contacts

Public ContactDrAKPrasath

Government Mohan Kumaramangalam Medical College Hospital Salem

gmkmchotacademics@gmail.com9342792264

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026