UnknownNot Applicable

Rhomboid Intercostal and Subserratum Plane Block for Minimally Invasive Esophagectomy

China96 participantsStarted 2023-03-01

Plain-language summary

The objective is to investigate the safety and effectiveness of rhomboid intercostal and subserratum plane (RISS) block for postoperative analgesia after minimally invasive McKeown esophagectomy (MIE-McKeown).

Who can participate

Age range

18 Years – 75 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: * Patients received MIE-McKeown surgery and were confirmed by postoperative pathology; Age 18-75 years old * body mass index (BMI) : 18.5\~23.9kg/m2; * American Society of Anesthesiologists (ASA) grade: Ⅰ\~Ⅱ; * Clear consciousness, no cognitive impairment; * Patients informed to participate in the study and signed informed consent. Exclusion Criteria: * Infection of the puncture site, abnormal platelet or coagulation function; * Patients with drug allergy involved in this study; * Long-term use of analgesic, sedative drugs or a history of heavy drinking; * Patients with chronic painful diseases; * With severe heart, liver, kidney and lung dysfunction; * Infectious diseases, blood, immune, circulatory system diseases; -Communication barriers, can not cooperate with the scale assessment; - * Other situations not suitable for this study.

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

Analgesic effect

Timeframe: 2, 6, 12, 24, and 48 hours after surgery

mean arterial pressure (MAP)

Timeframe: before anesthesia induction (T0)， before skin incision（T1）， 5 minutes after skin incision

Heart rate (HR)

Timeframe: before anesthesia induction (T0)， before skin incision（T1）， 5 minutes after skin incision

Trial details

NCT IDNCT06092944

SponsorLuo Fuchao

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-06-30

Contact for this trial

Luo fuchao, MD

+8613896658090 luokyyx@163.com

View on ClinicalTrials.gov More Esophagus Cancer trials

Who can participate

Age range

18 Years – 75 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.

What they're measuring

Analgesic effect

Timeframe: 2, 6, 12, 24, and 48 hours after surgery

mean arterial pressure (MAP)

Timeframe: before anesthesia induction (T0)， before skin incision（T1）， 5 minutes after skin incision

Heart rate (HR)

Timeframe: before anesthesia induction (T0)， before skin incision（T1）， 5 minutes after skin incision