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A Retrospective Analysis of Factors Associated with the Choice of Anaesthesia, Anaesthetic Outcomes and Postoperative Prognosis in Patients Undergoing Abdominal Hernia Repair

A Retrospective Analysis of Factors Associated with the Choice of Anaesthesia, Anaesthetic Outcomes and Postoperative Prognosis in Patients Undergoing Abdominal Hernia Repair

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128871
Enrollment
Unknown
Registered
2026-07-27
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

None

Interventions

Sponsors

Hebei Province Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients with clinically diagnosed abdominal hernia confirmed by physical examination and imaging, scheduled for elective open or laparoscopic hernia repair; 2.Aged >= 18 years old; American Society of Anesthesiologists (ASA) physical status classification I–III; 3.Complete and intact medical records covering preoperative anesthetic assessment, anesthesia induction and maintenance, intraoperative vital sign monitoring, postoperative recovery care and inpatient information without missing data; 4.Absence of absolute or relative contraindications to all types of anesthesia; smooth anesthesia induction and maintenance, without intraoperative conversion of anesthetic modalities or severe anesthesia-related adverse events; 5.Standardized clinical diagnosis and therapeutic regimens; full perioperative inpatient observation and rehabilitation after surgery, with complete prognostic outcome data.

Exclusion criteria

Exclusion criteria: 1.Patients receiving emergency abdominal hernia repair for incarcerated or strangulated hernias; 2.Patients complicated with severe dysfunction of vital organs (heart, lung, liver, kidney), as well as uncontrolled hypertension, diabetes mellitus and coagulation disorders; 3.Patients with history of anesthetic allergy, opioid dependence, cognitive dysfunction or poor compliance with clinical diagnosis and treatment; 4.Patients with missing core data including medical records, anesthetic records and intraoperative monitoring indicators, which cannot satisfy the requirements for statistical analysis; 5.Patients complicated with severe intraoperative surgical complications (massive hemorrhage, visceral injury) or severe anesthesia-related adverse events, whose postoperative prognosis cannot be evaluated; 6.Patients with self-discharge, inter-hospital transfer or loss to follow-up after surgery, leading to incomplete prognostic data involving postoperative complications and recovery duration.

Design outcomes

Primary

MeasureTime frame
Perioperative haemodynamics (mean arterial pressure, MAP; heart rate, HR);Usage of perioperative sedative and analgesic agents;

Secondary

MeasureTime frame
Postoperative nausea and vomiting (PONV), dizziness and pruritus;Intraoperative depth of anaesthesia (bispectral index, BIS);Postoperative blood oxygen saturation (SpO2) and respiratory rate (RR);

Countries

China

Contacts

Public ContactWang Guorui

Hebei Province Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine

13703334415@139.com+86 317 8266828

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026