UnknownNot Applicable

Rhomboid Intercostal Block Combined With Sub-Serratus Plane Block Versus Erector Spinae Plane Block

Egypt75 participantsStarted 2022-01-01

Plain-language summary

The aim of this study is to assess the quality of analgesic efficacy and improvement of pulmonary function in patients with fracture ribs receiving either continuous rhomboid intercostal block combined with sub-serratus block or continuous erector spinae plane block by comparing and evaluating the differences between the two techniques.

Who can participate

Age range

21 Years – 60 Years

Sex

ALL

See this in plain English?

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

Inclusion Criteria: * Adult patients between 21 - 60 years. * Patients with blunt chest trauma. * Multiple fracture ribs (at least 3 ribs). * Patients with acute trauma less than 48 hours. Exclusion Criteria: * Patients with major trauma outside the chest wall e.g., severe traumatic brain injury or major abdominal visceral injuries. * Patients with bilateral rib fractures. * Patients that are intubated and mechanically ventilated. * Pregnant Individuals. * Patients with local deformity or infection at the site of injection. * Sensitivity to local anesthetic drugs. * Patients with flail chest. * Patients with Suspected or diagnosed coagulopathy.

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

Total opioid analgesic consumption per day

Timeframe: 4 days

Trial details

NCT IDNCT05506761

SponsorTanta University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-01-01

Contact for this trial

Ahmed G. ElNawagy

01158170077 ahmed.nawagy@med.tanta.edu.eg

View on ClinicalTrials.gov More Rib Fractures trials