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Special liquid diet after C-Section may help sick moms recover faster

NCT ID NCT06164301

Knowledge-focused Sponsor: Ain Shams University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether giving a special liquid nutrition formula soon after C-section helps critically ill mothers in the ICU get enough protein and energy. 83 women participated, and researchers measured their protein intake and satisfaction with recovery. The goal was to see if this approach improves recovery within an Enhanced Recovery After Surgery (ERAS) program.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

83 people

The number who actually took part.

Started

Apr 2024

Finished

Mar 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

16 to 50 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Critically ill Female patients with cesarean section with or without hysterectomy that requires ICU admission pre or postoperative Exclusion Criteria: * Decompensated heart failure, * Known allergy * Tryptophan intolerance * known inborn errors of metabolism of proteins as alkaptonuria * severe hepatic dysfunction (failure) * severe renal dysfunction (failure) * severe coagulopathy or DIC * circulatory shock or hemodynamic instability * Lactose intolerance * G6PD deficiency

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Conditions

The condition(s) this trial relates to.

Critical Illness kwashiorkor nutritional deficiency disease Patient Satisfaction protein-energy malnutrition puerperal disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Critical illness Malnutrition in pregnancy Malnutrition; protein Patient satisfaction Postpartum disorder

Contacts and locations

Locations

  • Ain shams university

    Cairo, Cairo Governorate, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.