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Comparison of the Maternal Hemodynamic between Epidural Analgesia Delivery and Combined Spinal-Epidural Analgesia Delivery

Comparison of the Maternal Hemodynamic between Epidural Analgesia Delivery and Combined Spinal-Epidural Analgesia Delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180626040240N1
Enrollment
100
Registered
2018-08-01
Start date
2018-06-15
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

Analgesia for normal vaginal delivery.

Interventions

Intervention 1: Intervention group: Epidural analgesia The neuroaxial block is performed with epidural needle number 18 G . First, for the t

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Ability to have a normal vaginal delivery Existence of labor pain and the delivery is in the active phase. Pregnant mother wants to reduce labor pain it self. Consent of the patient and her husbend.

Exclusion criteria

Exclusion criteria: Maternal or spouse dissatisfaction. Inability of the pregnant to remain motionless while doing work(e.g. Parkinson disease). Coagulation disorder Increased intracranial pressure (SOL). Local infections at the puncture site History of sensitivity to analgesics and other medication used in this investigation Acute lesions of the CNS Hemodynamic Disorders (e.g. hypotension or Hypovolemia). Cardiovascular Diseases that reduce the cardiac output Embryonic distress. GA 40 Abnormal fetal presentations History of C/S or any surgery on the uterus History of any surgery on the uterus BMI> 40

Design outcomes

Primary

MeasureTime frame
Maternal blood pressure. Timepoint: 5 min before performing the analgesia and then 5, 10, 20,40, 60 min after and then every 30 min until the exit of the fetus. Method of measurement: With the use of a Barometer.;Maternal pulse rate. Timepoint: 5 min before performing the analgesia and then 5, 10, 20,40, 60 min after and then every 30 min until the exit of the fetus. Method of measurement: With the use of a monitor device.;Maternal Oxygen Saturation. Timepoint: 5 min before performing the analgesia and then 5, 10, 20,40, 60 min after and then every 30 min until the exit of the fetus. Method of measurement: With the use of a pulse oximetry.

Secondary

MeasureTime frame
Apgar score. Timepoint: Minuts 1 and 5. Method of measurement: Calculating.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohamad Mahdi Almiski

Tabriz University of Medical Sciences

dr.mahdi.almiski@gmail.com+98 41 3441 1230

Outcome results

None listed

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