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The Effect Of Spinal Anesthesia Drug to Prevent Maternal Hypotention

The effect of low dose Bupivacaine with fentanyl in spinal anesthesia for cesarean delivery to prevent maternal hypotension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201704183305N8
Enrollment
105
Registered
2017-04-28
Start date
2015-12-06
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Maternal hypotension. maternal hypotension syndrome

Interventions

Intervention 1: Control group: 10 mg 0.5% bupivacaine was injected into subarachnoid space. Intervention 2: Intervention Group1: 8 mg of bupivacaine 0.5 with 25 micrograms of fentanyl was injected int
Prevention
Control group: 10 mg 0.5% bupivacaine was injected into subarachnoid space.
Intervention Group1: 8 mg of bupivacaine 0.5 with 25 micrograms of fentanyl was injected into subarachnoid space.
Intervention Group2: 8 mg of bupivacaine 0.5% with 0.4 micrograms of Normal saline was injected into subarachnoid space

Sponsors

Vice chancellor research for Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: pregnant women, candidate for elective CS, in class I physical health classification of the American Society of Anesthesia (ASA). All women had singleton term pregnancies. Exclusion criteria: Mothers with a history of hypertension, diabetes, cardiovascular and cerebral diseases, known fetal anomaly, any kind of contraindications for spinal anesthesia, patients weighing over 100 kg and those with dificult tracheal intubation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Maternal blood presure. Timepoint: Maternal blood pressure was monitored and recorded every two minutes for the first 15 minutes following spinal anesthesia, and then every 5 minutes until completion of surgery. Method of measurement: Non invasive blood presure cuff.

Secondary

MeasureTime frame
Sensory level and motor block. Timepoint: After spinal anesthesia. Method of measurement: Sensory level was assessed using the tip of a needle sterilized with alcohol cotton, and motor block was assessed and recorded using Bromage Scale (BS) (BS=0, full knee and foot flexion; BS=1, ability to move knee; BS=2, ability to move feet only; BS=3, full motor block).;Pain. Timepoint: Pain level during surgery. Method of measurement: VAS (Visual analogues Scale).;Return of sensory and motor block. Timepoint: After Surgery. Method of measurement: Examination, Question & Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Hakimeh Alereza Amiri

Babol University of Medical Sciences

halereza@yahoo.com+98 11 3223 8284

Outcome results

None listed

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