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Postoperative Results of Early Versus On-demand Maternal Feeding After Cesarean Delivery

Postoperative Results of Early Versus On-demand Maternal Feeding After Cesarean Delivery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03349151
Enrollment
262
Registered
2017-11-21
Start date
2017-11-19
Completion date
2018-03-10
Last updated
2019-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Delivery, Feeding Patterns, Patient Satisfaction, Postoperative Nausea and Vomiting

Keywords

Postoperative maternal feeding, cesarean section

Brief summary

To compare early versus on demand maternal feeding after cesarean delivery regarding gastrointestinal complaints and patient's satisfaction.

Detailed description

Two hundred uncomplicated singleton term pregnancies who had caesarean section under regional anaesthesia will be included in our trial. Patients will be randomized to a soft food diet (honey, skimmed cheese, soup, mashed potatoe, pudding, grissini) served on postoperative 2nd hour or whenever they wanted to eat on return to the ward. Thirty minutes after they eat their meal, nausea, vomiting, ileus and distention will be questioned. Participants will be provided with the visual analogue scale (VAS), which will be presented with a statement explaining what was intended to measure. Patient satisfaction before discharge from hospital will be recorded by the patient by using a 100-mm VAS (0= minimum satisfaction, 100= maximum satisfaction). Time to first flatus passage and defecation will be recorded after the caesarean section.

Interventions

BEHAVIORALEarly feeding

Feeding on postoperative 2nd hour on return to the ward

BEHAVIORALOn- Demand feeding

Feeding whenever the patient asks for on return to the ward

Sponsors

Acibadem University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Prospective randomised

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Uncomplicated singleton term pregnancy * Planned or intrapartum uncomplicated cesarean section * Cesarean section under regional anesthesia

Exclusion criteria

* General anesthesia * History of bowel surgery * Prenatal diagnosis of fetal anomaly * Maternal disease * Intraoperative or immediate postoperative major complications

Design outcomes

Primary

MeasureTime frameDescription
Patient satisfactionOn postoperative day 2 before they are discharged from the hospital.The primary outcome is patient satisfaction before discharge from hospital, measured using a scale called visual analogue scale (VAS). It is a 100-mm long scale with adjectival descriptions at both end positions. There will be a statement explaining what was intended to measure. Participants will be asked to mark the VAS on the second they of the surgery before they are discharged from the hospital. On this scale 0= lack of satisfaction from the timing of having their meal after the surgery 100= full satisfaction from the timing of their meal after the surgery.

Secondary

MeasureTime frameDescription
Postoperative passage of flatus and defecationPostoperative day 0 to day 2.The participants will be asked to inform the nurse when they have their first passage of flatus and defecation.
Postoperative gastrointestinal complaintsThirty minutes after the surgeryThirty minutes after the surgery the nurse will question the patients if they have a complaint of nausea, vomiting or abdominal distention.
Postoperative pain medicationPostoperative from day 0 to day 2After the surgery the need for pain medication will be followed. The name of the medicine, the time when the pain killer was used, the dosage of the medicine will be recorded.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026