RecruitingNot Applicable

The Analgesic Efficacy of Vitamin B Complex in Critically Ill Obstetrics After Caesarean Section

Egypt100 participantsStarted 2024-05-25

Plain-language summary

We aim to investigate the value of vitamin B (B1, B6, B9, B12) on post-cesarean section analgesia in addition to the standard opioid-sparing multimodal regimen to achieve more robust analgesia with minimal side effects.

Who can participate

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Exclusion criteria

. Patient's Refusal to participate
. Known allergy to one or more of the given components.
. Disturbed conscious level.
. Prolonged or complicated surgery; defined by operative time of more than 90 min.
. Severe liver dysfunction or failure
. Severe renal dysfunction or failure.
. Severe thrombocytopenia; platelets less than 50

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

The total consumption of rescue analgesics in the first and second 24 hours after delivery

Timeframe: in the first 24 hours and in the second 24 hours (if stay is extended )

Pain score assessed by numerical pain scale after 24 hours from delivery.

Timeframe: 24 hours postoperative

Trial details

NCT IDNCT06446830

SponsorAin Shams University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-11-01

Contact for this trial

wessam selima, MD

01001958858 w.z.selima@med.asu.edu.eg

View on ClinicalTrials.gov More Analgesia trials

Who can participate

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Exclusion criteria

. Patient's Refusal to participate
. Known allergy to one or more of the given components.
. Disturbed conscious level.
. Prolonged or complicated surgery; defined by operative time of more than 90 min.
. Severe liver dysfunction or failure
. Severe renal dysfunction or failure.
. Severe thrombocytopenia; platelets less than 50