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Major Pelvic Hemorrhage in Complex Surgery

Management and Outcomes of Major Pelvic Hemorrhage in Patients Undergoing Complex Abdomino-Pelvic Surgery: A Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04264988
Enrollment
120
Registered
2020-02-11
Start date
2018-04-19
Completion date
2018-10-19
Last updated
2020-02-11

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

Conditions

Pelvic Bleeding

Brief summary

Hemorrhage is a challenging complication of pelvic surgery. In this study, the investigators aimed to analyze the causes, management, and outcomes of major pelvic hemorrhage in patients undergoing complex abdomino-pelvic surgery. Participants who had a major intraoperative pelvic hemorrhage during complex abdomino-pelvic surgery at 11 tertiary referral centers were included. Participant characteristics, causes of hemorrhage, management strategies, and outcomes including morbidity and mortality analyses were evaluated.

Interventions

PROCEDUREStopping of pelvic bleeding via several surgical methods

Those surgical methods were pelvic packing, electrocautery, energy devices, suturing, fastener, muscle welding, procoagulant chemicals, and combination of those

Sponsors

Bursa Medicana Hospital
CollaboratorUNKNOWN
Dokuz Eylul University
CollaboratorOTHER
Cukurova University
CollaboratorOTHER
Pamukkale University
CollaboratorOTHER
Ankara University
CollaboratorOTHER
TOBB University
CollaboratorUNKNOWN
Gazi University
CollaboratorOTHER
Baskent University
CollaboratorOTHER
Ege University
CollaboratorOTHER
Medipol University
CollaboratorOTHER
Gulhane Training and Research Hospital
CollaboratorOTHER_GOV
Acibadem University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Patients who had major pelvic bleeding during complex abdominopelvic surgery * Patients operated in hospitals where over 225 colorectal cases were performed every year

Exclusion criteria

* Patients operated for palliative intent

Design outcomes

Primary

MeasureTime frameDescription
Peri-operative outcomesWithin postoperative day 30Complication rate (Number of participants who had a complication divided by total number of participants)

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026