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Analgesic effects of subcutaneous of low dose Ketamine before and after cesarean section surgery

Analgesic effects of subcutaneous of low dose Ketamine before and after cesarean section surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013022012539N1
Enrollment
60
Registered
2013-08-17
Start date
2013-09-23
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

Pain. Acute Pain

Interventions

Intervention 1: Drugs: 1-Ketamine: Dose: 0.5mg/kg Number of using: Once Factory name: Rotex medica Manufacturing Country's Name: Germany Location prescribed: In place of incision Subcutaneously
Treatment - Drugs
Placebo
Drugs: 1-Ketamine: Dose: 0.5mg/kg Number of using: Once Factory name: Rotex medica Manufacturing Country's Name: Germany Location prescribed: In place of incision Subcutaneously Administr
Drug: Normal Saline Dose: 10 ml Number of using: Once Factory name: Daroupakhsh Manufacturing Country's Name: Iran Location prescribed: In place of incision Subcutaneously Administration t
Drugs: 1-Ketamine: Dose: 0.5mg/kg Number of using: Once Factory name: Rotex medica Manufacturing Country's Name: Germany Location prescribed: In place of incision Subcutaneously Administrat

Sponsors

Vice chancellor for research, Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: - The patient's satisfaction – Age between 20 and 40 years old - ASA class I & II Exclusion criteria: - The lack of patient's satisfaction to spinal anesthesia - History of hypnotics or narcotics throughout 24 hours before the surgery - History of drug abuse, or alcohol- dependency - Contraindication of Ketamine - Contraindications of Spinal Anesthesia( Patient refusal ; Infection at the site of planned needle puncture ; Elevated intracranial pressure and Bleeding diathesis)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 1,2,4,6,12,18 and 24 hours after surgery. Method of measurement: Visual Analogue Scale.

Secondary

MeasureTime frame
Opioid Consumption. Timepoint: 24 hours after surgery. Method of measurement: Milligram.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Aslani

Ahvaz Jundishapur University of Medical Sciences

aslani.m@ajums.ac.ir+98 61 1332 5869

Outcome results

None listed

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