Skip to content

Clinical observation of glycopyrronium bromide and penehyclidine hydrochloride in laparoscopic cholecystectomy

Clinical observation of glycopyrronium bromide and penehyclidine hydrochloride in laparoscopic cholecystectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107519
Enrollment
Unknown
Registered
2025-08-13
Start date
2025-01-06
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

Gallbladder stones

Interventions

The control group (group C):Saline (medicine)
The glycopyrrolate group(group G):Group G was injected with 4 µg/kg of glycopyrrolate intravenously,
Penehyclidine hydrochloride group (group P):Penehyclidine hydrochloride

Sponsors

The First People’s Hospital of Jingzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1.Sex is not limited, age 18~64 years old; 2.ASA classification: Grade I-II, no airway obstruction; 3.BMI=18~30 kg/m2; 4.Patients undergoing elective laparoscopic cholecystectomy; 5.Complete and accurate clinical information. 6.No significant cardiac, pulmonary, hepatic, renal or other vital organ dysfunction; 7.The patients and their families were fully aware of the process of this study and were willing to sign the informed consent and follow the order strictly as required.

Exclusion criteria

Exclusion criteria: 1. Unconsciousness or cognitive impairment; 2. Allergy to anticholinergic drugs and their constituents; 3. Poorly controlled hypertension (SBP > 160 mmHg or DBP >100 mmHg); 4. Patients with atrioventricular block, bradycardia, severe arrhythmia and unstable angina pectoris; 5. Patients with glaucoma; 6. Unconsciousness or cognitive impairment; 7. History of postoperative nausea, vomiting and motion sickness; 8. Pregnancy or lactation; 9. Participated in other drug clinical trials within the past 3 months; 10. Patients who refused to participate in the study.

Design outcomes

Primary

MeasureTime frame
Incidence of nausea and vomiting 24h after surgery;

Secondary

MeasureTime frame
HR and MAP;Oral glandular secretion, length of stay in the PACU;Dry mouth (xerostomia), delirium, urinary retention, and time to first venting;Hypotension, bradycardia;Incidence of nausea and vomiting at 1 h postoperatively.;

Countries

China

Contacts

Public ContactRui Xia

The First People’s Hospital of Jingzhou

879560350@qq.com+86 18972161338

Outcome results

None listed

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