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Comparing the effects of bupivacaine and ropivacaine in the casarean section.

Comparing the effects of bupivacaine and ropivacaine on the patients undergoing cesarean section in spinal anesthesia

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190529043751N1
Enrollment
60
Registered
2019-07-08
Start date
2019-04-04
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

cesarean. Complications of anesthesia during labor and delivery

Interventions

Intervention 1: Ropivacaine group: Ropivacaine 1%( 15mg) ) (manufactured by Dei Fratelli Societa Di Eserciozio SpA C & Molteni L, Italy) will be injected during surgery. Intervention 2: Bupivacaine g

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Term pregnancy (over 37 and less than 42 weeks) Elective cesarean section 20-40 years Weight between 65 and 95 kg Height between 155 and 175 cm ASA class I,II

Exclusion criteria

Exclusion criteria: Preterm and post term Abnormalities and problems of placenta or fetus Allergy to local anesthetics Spinal anesthesia contraindications

Design outcomes

Primary

MeasureTime frame
Motor block duration. Timepoint: Every 5 minutes in the first 32 minutes and then at 12-minute intervals until the end of surgery. Method of measurement: Modified bromage scale.;?Sensory block duration. Timepoint: Every 5 minutes in the first 32 minutes and then at 12-minute intervals until the end of surgery. Method of measurement: pin prick.

Secondary

MeasureTime frame
Blood pressure. Timepoint: Every 5 minutes before injection until delivery and then every 15 minutes until discharge from the recovery room. Method of measurement: Non-invasive Blood Pressure (NIBP).;Heart rate. Timepoint: Every 5 minutes before injection until delivery and then every 15 minutes until discharge from the recovery room. Method of measurement: ECG.;Analgesia. Timepoint: In the beginning and end of surgery and, when discharging from recovery room. Method of measurement: Visual analogues Scale.;Postoperative Clinical complications. Timepoint: Until 24 hours after discharge from the recovery room. Method of measurement: Examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRaziyeh Homayoon

Ahvaz University of Medical Sciences

raziyeh.homayoon@yahoo.com+98 61 3222 2114

Outcome results

None listed

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