At a glance
ClinicalIndex Comparison RecordN/ACompleted· 42 enrolled
Drug / intervention
Bupivacaine-fentanyl +1 moredrug
Likely dose
Bupivacaine-fentanyl 2,5 mlfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Comparative Study of Fractionated Vs Single Dose Injection for Spinal Anesthesia During Caesarean Section in Patients With Pregnancy-Induced Hypertension
In Brief
A clinical study evaluating Bupivacaine-fentanyl for Pregnancy Induced Hypertension. Completed, enrolled 42 participants across 1 site.
Detailed Summary
The aim of this study was to compare haemodynamic changes, total dose of ephedrin requirement, and level of sensory blockade between fractionated dose and single dose spinal anesthesia injection in obstetric patients with pregnancy-induced hypertension who underwent Caesarean section
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPregnancy Induced Hypertension
CountriesIndonesia
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartJan 2018
Primary CompletionApr 2018
Study CompletionMay 2018
First PostedOct 2018
TodayJul 2026
First PostedOct 3, 2018
Enrollment StartJan 1, 2018
Primary CompletionApr 30, 2018
Study CompletionMay 31, 2018
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 7.7 years ago
Interventions
Bupivacaine-fentanyldrug
2,5 ml total anesthetic drug dose were given with 0.2 ml/second rate, and subjects were asked to remain sitted for 90 seconds
Bupivacaine-fentanyldrug
1,5 ml of total anesthetic drug dose followed by 1 ml remaining dose after 90 s interval were given