Preclinical research based on self-developed precise quantitative pain measurement device

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037026

Enrollment

Unknown

Registered

2020-08-26

Start date

2021-10-01

Completion date

Unknown

Last updated

2020-09-28

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

Conditions

Pain

Interventions

experimental group:Accurate quantitative pain measurement device was used for pain assessment

control group:VAS scoring was used for pain assessment

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1.Patients requiring abdominal surgery; 2.Above 18 years of age.

Exclusion criteria

Exclusion criteria: 1. Patients who are participating in other clinical trials; 2. Children, dementia, consciousness disorders and other patients who do not accurately judge the degree of pain or have language impairment; 3. Patients with severe coagulation dysfunction or taking anticoagulant drugs; 4. Patients with visceral pain; 5. The researchers believe that other reasons are not suitable for the patients in the clinical trial.

Design outcomes

Primary

Measure	Time frame
Pain relief;	—

Countries

China

Contacts

Public ContactZui Zou

Changzheng Hospital, The Second Military Medical University

zouzui1980@163.com+86 18621122799

Outcome results

None listed

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