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Tegileridine Pretreatment for the Prevention of Fentanil-Induced Cough During Anesthesia Induction: A Clinical Study

Tegileridine Pretreatment for the Prevention of Fentanil-Induced Cough During Anesthesia Induction: A Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115512
Enrollment
Unknown
Registered
2025-12-26
Start date
2025-12-27
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Patients undergoing general anesthesia with fentanil-induced tracheal intubation

Interventions

Group T (Tiglyldine Group):0.5 mg of tigelidine is prepared in 5 ml of solution iv.
Group S (Normal Saline Control Group):5 ml of 0.9% normal saline iv.

Sponsors

Weifang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. ASA class I-III; 2. Aged 18-65 years; 3. Require the use of fentanil for endotracheal intubation under general anesthesia induction; 4. Voluntarily signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. Drug allergy; 2. Sinus bradycardia; 3. Severe neurological, respiratory, or cardiovascular disease; 4. Anesthetic drug dependence; 5. Hepatic or renal dysfunction; 6. Gallbladder surgery; 7. Pregnancy, lactation, or delivery surgery; 8. Patients with upper respiratory tract infection within 2 weeks or other conditions that may induce spontaneous coughing.

Design outcomes

Primary

MeasureTime frame
The incidence of cough following fentanil injection;

Secondary

MeasureTime frame
Number of patients with coughs of different severity grades;Blood pressure;Heart rate;Pulse oxygen saturation;Other side effects associated with tiglyldine and fentanil;

Countries

China

Contacts

Public ContactZhang Shaojie

Weifang People's Hospital

zsj3522890@sdsmu.edu.cn+86 188 6366 3775

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 17, 2026