Skip to content

Clinical study on related factors of tourniquet pain

Clinical study on related factors of tourniquet pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048525
Enrollment
Unknown
Registered
2021-07-09
Start date
2021-07-12
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

tourniquet pain

Interventions

Case series:none

Sponsors

The First Affiliated Hospital of University of science and technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. ASA grade I or II; 2. Patients who need tourniquet and the operation time is more than 20 minutes; 3. Aged > 18 years; 4. BMI 18.5~24.9 kg/m2.

Exclusion criteria

Exclusion criteria: 1. Abnormal liver and kidney function, with a history of chronic diseases such as hypertension and coronary heart disease; 2. Previous blood diseases such as peripheral vascular disease, thrombotic disease, severe atherosclerosis; 3. Those who have a history of anxiety or depression and are taking sedatives and tranquilizers; 4. Participants with communication barriers, unable to cooperate with inspection, re-examination or lost to follow-up; 5. Patients with contraindications to nerve block; 6. Patients with a history of chronic pain and taking painkillers; 7. Patients with skin damage at the site where the tourniquet is used or who cannot use the tourniquet for other reasons.

Design outcomes

Primary

MeasureTime frame
Pain sensitivity;

Countries

China

Contacts

Public ContactKang Fang

The First Affiliated Hospital of University of science and technology of China

kangfang199771@163.com+86 18155127799

Outcome results

None listed

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