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Correlation between pain sensitivity and postoperative sleep disorders in non-elderly patients undergoing intestinal polypectomy under general anesthesia

Correlation between pain sensitivity and postoperative sleep disorders in non-elderly patients undergoing intestinal polypectomy under general anesthesia

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300078614
Enrollment
Unknown
Registered
2023-12-14
Start date
2023-12-01
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Shihezi University

Interventions

High pain sensitivity group (H group):None
Low pain sensitivity group (L group):None

Sponsors

The First Affiliated Hospital of Medical College of Shihezi University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: (1) Age of 18-64 years old; (2) ASA grade I-III; (3) be able to cooperate with the evaluation of various rating scales.

Exclusion criteria

Exclusion criteria: (1) sleep disorder with PSQI score > 7; (2) HADS-A > 7 points or HADS-D > 7 points for anxiety or depression; (3) Body mass index (BMI) > 30kg/?; (4) complicated with serious important organ function diseases (such as heart, brain, liver, kidney, etc.); (5) continuous abuse of sedatives, analgesics, alcohol and other drugs known to affect sleep; (6) preoperative history of rheumatoid arthritis, central or peripheral nervous system diseases, skin ulceration, scar paresthesia, and diseases that may affect pain perception; (7) history of cognitive impairment, psychiatric or epileptic disorders; (8) Sick sinus syndrome and severe bradycardia (<50 beats/minute) or atrioventricular block of second degree or above.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative sleep disorders;Sleep staging on the first postoperative night;Sleep efficiency on the first postoperative night;The first night after awakening;After the first night sleep incubation period;

Secondary

MeasureTime frame
Operating time; Awakening time;Drug add > 3 times;Incidence of hypotension;Incidence of bradycardia;Incidence of respiratory depression;Incidence of nausea and vomiting;Incidence of abdominal pain and distension;Incidence of lethargy and fatigue;Incidence of dizziness and headache;To sleep time before sleep monitoring patients after surgery;

Countries

China

Contacts

Public ContactPan Ziyan

Shihezi University;The First Affiliated Hospital of Medical College of Shihezi University

1597940172@qq.com+86 187 9975 2669

Outcome results

None listed

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