Could a Pre-Surgery drink boost C-Section recovery?
NCT ID NCT07204795
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether drinking a clear carbohydrate-rich beverage two hours before a planned C-section can help women recover faster and feel less hungry, thirsty, or anxious. One hundred women will be randomly assigned to get either the carbohydrate drink or plain distilled water. Researchers will measure recovery scores at 24 and 48 hours after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- carbohydrate-rich clear drink
- What this could lead to
- If it works, this could lead to a simple way to improve comfort and recovery after planned C-sections.
- What could go wrong
- This is a small, early-phase trial with only 100 participants, so results may not apply to all women. The drink may not show a meaningful benefit over water.
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
-
About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
May 2025
- Expected to finish
-
May 2026
An estimate. End dates often move.
- 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
-
18 years and older
- Sex
-
Female participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: Age ≥18 years Scheduled for elective cesarean section under neuraxial anesthesia Gestational age ≥37 weeks Exclusion Criteria: Contraindication to neuraxial anesthesia Age \<18 years Refusal to participate in the study Obesity Hiatal hernia Intestinal obstruction Gastroesophageal reflux disease (GERD) Diabetes mellitus Fetal anomalies Eclampsia or preeclampsia Substance abuse Chronic pain conditions
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Cesarean section are added.
By submitting, you agree to our Terms of use
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Ataturk University Research Hospital
RECRUITINGErzurum, 25700, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Effectiveness of health educational program for primigravida women in reducing the rate of unnecessary cesarean section
- Two common drugs face off to shield mothers from a dangerous drop in blood pressure
- Can simple recovery checklists after cesarean boost patient well-being?
- Can we predict severe pain after C-Section?
- Can a slower oxytocin infusion prevent dangerous blood pressure drops in C-Sections?
- Can an AI chatbot calm nerves before a C-Section as well as a doctor?