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The impact of nebulized inhalation of penehyclidine hydrochloride on pulmonary function in obese patients with OSA after laparoscopic surgery

The impact of nebulized inhalation of penehyclidine hydrochloride on pulmonary function in obese patients with OSA after laparoscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112331
Enrollment
Unknown
Registered
2025-11-12
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Obesity

Interventions

Control group (Group C):Nebulized inhalation of 5ml physiological saline solution
Pentachloroquine hydrochloride group (PHC group):Nebulized inhalation of 0.5mg of pentachloroquine hydrochloride (diluted to 5ml with physiological saline)

Sponsors

The First Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years; 2. ASA (American Society of Anaesthesiologists) physical status classification II–III; 3. Body Mass Index (BMI) >=35 kg/m²; 4. Sleep apnoea and hypopnoea index (AHI) >=15 events per hour; 5. Patients undergoing elective laparoscopic sleeve gastrectomy; 6. No history of drug allergies or abnormal anaesthesia; 7. Tracheal tube removal planned to occur in the operating theatre.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of ALI/ARDS within the past three months, those with severe pulmonary dysfunction (SpO2 = 3), or rapid arrhythmias; 3. Patients with severe hepatic or renal impairment (requiring renal replacement therapy, Child-Pugh class C); 4. Patients with moderate to severe symptomatic prostatic hypertrophy or narrow-angle glaucoma; 5. Patients who have used inhaled beta-2 agonists, anticholinergic drugs, and/or glucocorticoids within one month prior to surgery; 6. Patients who have participated in other drug trials within one month prior to surgery; 7. Patients unable to cooperate with inhalation therapy; 8. Known hypersensitivity to propofol hydrochloride; 9. Patients planned for transfer to the ICU post-operatively; 10. Patients refusing to participate in the clinical trial.

Design outcomes

Primary

MeasureTime frame
Area Under the Curve (AUC) of Driving Pressure (DP) at 5 minutes after pneumoperitoneum (T1), 20 minutes after pneumoperitoneum (T2), 35 minutes after pneumoperitoneum (T3), and at the end of pneumoperitoneum (T4).;

Secondary

MeasureTime frame
Airway peak pressure;Area under the airway peak pressure curve;Dynamic lung compliance ;Area under dynamic lung compliance curve;Alveolar arterial oxygen pressure difference (A-aO2);Alveolar arterial oxygen pressure difference (A-aO2);The incidence of postoperative 48 hour hypoxemia;Pulmonary ultrasound score(LUS);Incidence of atelectasis;Adverse reaction rate;Oxygenation index (OI);Oxygenation index (OI);Serum SP-A concentration;Serum SP-A concentration;

Countries

China

Contacts

Public ContactGuo Qiongmei

The First Hospital of Hebei Medical University

guo-qiongmei@163.com+86 155 1166 0729

Outcome results

None listed

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