Skip to content

Effects of Remimazolam versus Propofol on Perioperative Stress Response and Quality of Postoperative Recovery in Obese Patients Undergoing Bariatric Surgery: A Single-Center Randomized Non-Inferiority Controlled Trial

Effects of Remimazolam versus Propofol on Perioperative Stress Response and Quality of Postoperative Recovery in Obese Patients Undergoing Bariatric Surgery: A Single-Center Randomized Non-Inferiority Controlled Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106338
Enrollment
Unknown
Registered
2025-07-22
Start date
2025-07-22
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None

Interventions

R group:Anesthesia induction:Group R was intravenously injected with remazolam besylate 0.3mg/kg (injection time >30s) Anesthesia maintenance with Remazolam besylate (0.2 ~ 1.0 mg/kg/h)
P group:Anesthesia induction:Intravenous propofol 2 mg/kg (0.5 ml/s) in Group P Anesthesia maintenance with Propofol (2 to 4 mg/kg/h, group P)

Sponsors

Jinan Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Paients with intravenous aspiration combined under general anesthesia in laparoscopic sleeve gastrectomy wereslective , age 18-60 years, ASAI ~ II, BMI>=30kg/m^2

Exclusion criteria

Exclusion criteria: (1) Preoperative diagnosis of airway difficulties (Mallampati grade =III) or sleep apnea syndrome;(2) severe neuropsychiatric disorders and cognitive dysfunction;(3) Allergic history of benzodiazepines;(4) significant cardiopulmonary instability (heart failure, acute lung injury, hypovolemia or sepsis) and renal or liver dysfunction;(5) Contraindications to remazolam (such as myasthenia gravis, schizophrenia, major depression);(6) have used opioids or benzodiazepines in the past month;(7) Drug or alcohol abuse;(8) Pregnant or breastfeeding patients and women who plan to become pregnant within 3 months.

Design outcomes

Primary

MeasureTime frame
QoR-15 score of POD1;Hemodynamic index;

Secondary

MeasureTime frame
quality of recovery;IL-6;TNF-a;GLU;Lactic acid;norepinephrine;Epinephrine;Pain intensity;Adverse drug events;

Countries

China

Contacts

Public ContactRuimei Yuan

Jinan Central Hospital; Central Hospital Affiliated to Shandong First Medical University

subave@sina.cn+86 155 5412 7179

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026