Skip to content

Comparison Apotel and suppositories diclofenac on pain relief after cesarean section

Comparison Apotel and suppositories diclofenac on pain relief after cesarean section among primiparous women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015092513336N2
Enrollment
120
Registered
2016-04-22
Start date
2015-11-06
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 after cesarean. Delivery by caesarean section, unspecified

Interventions

Intervention 1: In the intervention group, One hour and thirty minutes after spinal anesthesia and before Back pain after surgery were given 50 mg of pethidine vial. And then expressed the need for an
Treatment - Drugs
In the intervention group, One hour and thirty minutes after spinal anesthesia and before Back pain after surgery were given 50 mg of pethidine vial. And then expressed the need for analgesic vial Apo

Sponsors

Research Council of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: minimum education subjects as reading and writing, lives with his wife, a singleton pregnancy, gestational age 38 to 42 weeks, primiparous women, healthy baby and the first minute Apgar score 7-10, the same method cesarean delivery and a cross-section (skin and uterus), mothers with vital signs are favorable. Exclusion criteria: The presence of unusual complication of surgery (bladder trauma or other injury during surgery), preoperative fever, Smoking and drug addiction, hysterectomy Associated with cesarean, suffering from medical disorders (diabetes, hypertension, heart disease and vascular, renal, pulmonary, gastrointestinal, thyroid, immune disorders, infectious, psychiatric, metabolic disorders, electrolyte and irritable bowel syndrome), sensitivity to paracetamol, liver and kidney function decline, chronic alcoholism, chronic malnutrition or dehydration, taking probenecid or Sylasyd year or drugs are enzyme induction.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain of cesarean section. Timepoint: before the intervention until the 24 hours after intervention. Method of measurement: McGill Pain Questionnaire short.

Secondary

MeasureTime frame
Physical activity and psychosocial. Timepoint: 12 and 24 hours after cesarean section. Method of measurement: Interview form Pain interference with physical activity and psychosocial.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Aradmehr

Mashhad University of Medical Sciences

maryam.aradmehr@yahoo.com+98 51 5522 1005

Outcome results

None listed

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