Skip to content

Clinical trials of Comparison the effect of two methods, patient controlled analgesia and non steroidal anti inflammatory drugs after elective cesarean section

Clinical trials of Comparison the effect of two methods, patient controlled analgesia and non steroidal anti inflammatory drugs after elective cesarean section

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014091619197N1
Enrollment
100
Registered
2014-10-29
Start date
2014-08-28
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

postoperative pain. -

Interventions

Intervention 1: In the intervention group, namely injection by pump, analgesic pump contains 20 milligrams Morphine, which is diluted with normal saline to a volume of 100 cc. were injected by the pat
Treatment - Drugs
In the control group, whenever there analgesics were needed 100 milligrams Diclofenac was injected intramuscularly or Diclofenac suppository was used in turn (according to the available protocols).
In the intervention group, namely injection by pump, analgesic pump contains 20 milligrams Morphine, which is diluted with normal saline to a volume of 100 cc. were injected by the patients at injecti

Sponsors

Investigator
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 20 to 35, no history of cesarean surgery, not suffering from chronic pain, BMI less than 30, no sensitivity to opioids drugs, chronic diseases and patient's written consent. Exclusion criteria: a history of addiction to opioids, history of liver and kidney diseases, the existence of mental illness verifiy by a physician and lack of interest or withdrawal during the conduction of the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: every 6 hours after intervention. Method of measurement: visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Ahmadi

Sadjad hospital

majid.ahmadi@muk.ac.ir; ahmadimajid1365@gmail.com; majid.ahmadi1986@yahoo.com+98 83 3726 0606

Outcome results

None listed

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