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The Effect of early mouth feeding on the post-cesarean pain

The effects of early mouth feeding on the amount of pain in elective cesarean patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170110031865N3
Enrollment
126
Registered
2018-01-30
Start date
2017-03-21
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. Pain and other conditions associated with female genital organs and menstrual cycle

Interventions

Intervention 1: intervention group: Patients in the intervention group (early feeding with liquid diet) will be placed in sitting position 6 hours after surgery. Mouth feeding, Initially, 30 ml equals
intervention group: Patients in the intervention group (early feeding with liquid diet) will be placed in sitting position 6 hours after surgery. Mouth feeding, Initially, 30 ml equals to half of a gl
Control group: Patients in the control group will be treated according to the routine care. Meaning they will lie down on the back position for 12 hours without eating or drinking anything. The amoun

Sponsors

Vice Chancellor for research and technology of Kurdistan University of Medical Sciences
Lead Sponsor
Sanandaj University of Medical Sciences
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: women with singleton pregnancies gestational age 38 to 42 weeks elective cesarean (History: at least another previous Cesarean) surgery with a cross-section of the abdomen and spinal anesthesia vital signs within normal non-smoker and no addiction to drugs lack of any history of abdominal surgery other than caesarean Child alive Willing to participate in the study

Exclusion criteria

Exclusion criteria: patients giving up for any reason medical disorders and Midwifery (diabetes , anemia, high blood pressure, heart disease, cardiovascular, renal, pulmonary, gastrointestinal, thyroid, immune disorders, infectious, psychiatric, metabolic disorders, electrolyte and irritable bowel syndrome)

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Arrival, 6,12,18 and 24 hours after surgery. Method of measurement: Visual Analoge Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactzahra rashidei

Kurdistan University of medical sciences

zrashidei@yahoo.com+98 87 3872 2930

Outcome results

None listed

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