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Comparison of Preemptive Effect of Gabapentine and Intra techal Fentanyl on Post operative Pain after Caesarean Surgery.

Comparison of Preemptive Effect of Gabapentine and Intra techal Fentanyl on Post operative Pain after Caesarean Surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201202241936N8
Enrollment
60
Registered
2012-03-01
Start date
2012-03-19
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

Post operative pain. Complication of anaesthesia during labour and delivery, unspecified

Interventions

Intervention 1: In case group all the patients receive spinal anesthesia with bupiuvacaine .05% up to 2 milliliter.in this group all the patients receive 300 milligrams gabapentin orally 2 hours befor
Treatment - Drugs
In case group all the patients receive spinal anesthesia with bupiuvacaine .05% up to 2 milliliter.in this group all the patients receive 300 milligrams gabapentin orally 2 hours before surgery as pre
All the patient in control group receive 15 micrograms of fentany as pain protocol plus bupiuvacaine .05% up to 2 milliliter intratechaly

Sponsors

Bushehr University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the entire patient candidates for elective cesarean age between 20 till 40 that accept to come to study are inclusion criteria. Exclusion criteria: history of sensitivity to gabapentin; patient with hepatic and renal problem; history of epilepsy; patients that received analgesic 8 hours before surgery; patients with psychological problem; history of sensitivity to opioids and any situation that made regional anesthesia contraindicated.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Post operative pain. Timepoint: First 24 hours. Method of measurement: Observation.;Analgesic demands. Timepoint: First 24 hours. Method of measurement: Observation.

Secondary

MeasureTime frame
Patients' statisfication. Timepoint: First 24 hours. Method of measurement: Question.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Abdolreza Najafi Anaraki

Bushehr University of Medical Science

DR.NAJAFIANARAKI@GMAIL.COM+98 77 1252 2417

Outcome results

None listed

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