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Comparison of febrile morbidity between use and disuse intraoperative topical absorbable hemostatic agents in patient underwent abdominal hysterectomy: a retrospective cohort study

Comparison of febrile morbidity between use and disuse intraoperative topical absorbable hemostatic agents in patient underwent abdominal hysterectomy: a retrospective cohort study

Status
Unknown
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20230910003
Enrollment
316
Registered
2023-09-10
Start date
2018-01-01
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

febrile morbidity between use and disuse intraoperative topical absorbable hemostatic agents in patient underwent abdominal hysterectomy febrile morbidity, intraoperative topical absorbable hemostatic agents, abdominal hysterectomy

Interventions

usese intraoperative topical absorbable hemostatic agents in patient underwent abdominal hysterectomy,disusese intraoperative topical absorbable hemostatic agents in patient underwent abdominal hyster
Prevention,Prevention
usese intraoperative topical absorbable hemostatic agents,disuse intraoperative topical absorbable hemostatic agents

Sponsors

khonkaen university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
1 Years to 90 Years

Inclusion criteria

Inclusion criteria: All woman who underwent abdominal hysterectomy

Exclusion criteria

Exclusion criteria: Patients were underlying including chronic inflammation disease, coagulopathy, SLE, HIV, chronic hepatitis and connective tissue disease Patients were diagnosed prior or during intraoperative infection such as intraabdominal abscess Patients were used others intraoperative topical absorbable hemostatic agents excepts Surgicel Fibrillar Patients were not be received appropriate prophylaxis antibiotics Patient documents were not completely registered information

Design outcomes

Primary

MeasureTime frame
febrile morbidity at early 24 hours after end of the intervention hospital database

Secondary

MeasureTime frame
reoperation, vaginal cuff cellulitis and vaginal cuff dehiscence at 30 days after end of the intervention hospital database

Countries

Thailand

Contacts

Public Contactnititorn khantawichai

khonkaen university

abcdeton_412@hotmail.com66980970807

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026