Skip to content

Pretreatment with Remimazolam Supresses Cough Induced by Sufentanil during Induction of General Anesthesia:A Prospective, Randomized, Blind Trial

Pretreatment with Remimazolam Supresses Cough Induced by Sufentanil during Induction of General Anesthesia:A Prospective, Randomized, Blind Trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086733
Enrollment
Unknown
Registered
2024-07-09
Start date
2024-07-15
Completion date
Unknown
Last updated
2024-07-15

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

Conditions

Sufentanil-induced cough

Interventions

Remazolam group (group R):Pretreating with 0.02mg/kg (5ml) remazolam before induction of general anesthesia
Control group:Pretreating with 5ml of saline before induction of general anesthesia

Sponsors

The People's Hospital of Chaozhou City
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Select 106 patients undergoing elective gynecologic surgery under general anesthesia at the People's Hospital of Chaozhou City from July 2024 to February 2025.The American Association of Anesthesiologists (ASA) grade I-II, aged 18-60 years old, BMI 18~30 kg/m2.

Exclusion criteria

Exclusion criteria: ? Patients preexisting severe cardiovascular, brain, lung, liver, kidney or nervous system diseases; ? Patients allergic to opioids, diazepines, and propofol; ? Patients suspiciously abusing or addicted to sedative or narcotic analgesic drug; ? History of smoking, asthma, or chronic cough; ? History of upper respiratory tract infection 2 weeks before surgery; ? Patients receiving angiotensin-converting enzyme inhibitors, bronchodilators, or steroids 2 weeks before surgery; ? Patients with modified Mallampati rating IV or predicted respiratory difficulties;Patients with modified Mallampati rating IV or predicted respiratory difficulties; ? Serious treatment-related complications unrelated to drug trials occurring during the treatment of patients, including massive bleeding that difficult to treat, death and so on; ? Patients participating in other drug trials 3 months before surgery; ? Patients refusing cooperate or asking to withdraw from the study.

Design outcomes

Primary

MeasureTime frame
Cough;

Secondary

MeasureTime frame
Mean arterial pressure;Pulse oxygen saturation;Heart rate;

Countries

China

Contacts

Public ContactYe Haoling

The People's Hospital of Chaozhou City

770184606@qq.com+86 136 7143 2364

Outcome results

None listed

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