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A clinical observational study of preoperative salivary cortisol levels in predicting acute pain after laparoscopic hysterectomyperative acute pain

A clinical observational study of preoperative salivary cortisol levels in predicting acute pain after laparoscopic hysterectomyperative acute pain

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300074327
Enrollment
Unknown
Registered
2023-08-03
Start date
2023-08-10
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

postoperative acute pain

Interventions

Observation group:N/A

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 18~65 years old; ASA Classes I-III; Body mass index 18-30kg/m2; laparoscopic hysterectomy under general anesthesia; No history of chronic pain disease, psychiatric illness, severe physical illness, or dysfunction of vital organs; Patients who volunteered to participate in this study

Exclusion criteria

Exclusion criteria: 1. Refuse to accept research; 2. Have a history of severe mental illness or chronic pain; 3. Communication and cognitive impairment, history of alcohol and drug abuse; 4. History of severe trauma or surgery within the past year; 5. Adrenal gland disease, patients who have received hormone or steroid therapy in the past 6 months are excluded;

Design outcomes

Primary

MeasureTime frame
Salivary cortisol;NRS;

Secondary

MeasureTime frame
PSQI;STAI;

Countries

China

Contacts

Public ContactJu Gao

Northern Jiangsu People's Hospital

gaoju_003@163.com+86 180 5106 3988

Outcome results

None listed

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