NCT05430659

Brief Summary

After review literature, Siriraj hospital has not unanimous protocol to guide proper preoperative anemia and blood transfusion. This retrospective study will review non-cardiac surgery cases and collect data such as demographic data, surgical procedures, anesthetic techniques, preoperative hemoglobin level, intraoperative estimate blood loss, blood transfusion, and post operative complication in Siriraj hospital which has many patients undergo various operations. This study can be model to develop preoperative anemia management guideline in Siriraj Preanesthesia Assessment Center (SIPAC), Siriraj hospital and reduce risk and adverse outcomes after blood transfusion in the future.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,268

participants targeted

Target at P75+ for all trials

Timeline
7mo left

Started Jul 2022

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress87%
Jul 2022Dec 2026

First Submitted

Initial submission to the registry

June 15, 2022

Completed
9 days until next milestone

First Posted

Study publicly available on registry

June 24, 2022

Completed
7 days until next milestone

Study Start

First participant enrolled

July 1, 2022

Completed
4.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

March 6, 2026

Status Verified

June 1, 2025

Enrollment Period

4.3 years

First QC Date

June 15, 2022

Last Update Submit

March 4, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Operation with intraoperative blood loss of more than 500 ml

    Operation with intraoperative blood loss of more than 500 ml

    Day of surgery

Secondary Outcomes (1)

  • Risks associated with intraoperative blood loss of more than 500 ml

    Day of surgery

Study Arms (2)

EBL equal or more than 500 ml

The intraoperative estimated blood loss equal or more than 500 ml

Other: observational study

EBL less than 500 ml

The intraoperative estimated blood loss less than 500 ml

Other: observational study

Interventions

Retrospective observational study

EBL equal or more than 500 mlEBL less than 500 ml

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients undergoing surgical procedures consist of head/neck surgery, general surgery, urologic surgery, vascular surgery, neurologic surgery, orthopedic surgery, otolaryngologic surgery and gynecologic surgery.

You may qualify if:

  • Patients undergoing surgical procedures consist of head/neck surgery, general surgery, urologic surgery, vascular surgery, neurologic surgery, orthopedic surgery, otolaryngologic surgery and gynecologic surgery.

You may not qualify if:

  • Patients don't have target data or losing of interesting document.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Siriraj hospital

Bangkok, Bangkok, 10700, Thailand

Location

MeSH Terms

Conditions

Blood Loss, Surgical

Interventions

Observation

Condition Hierarchy (Ancestors)

HemorrhagePathologic ProcessesPathological Conditions, Signs and SymptomsIntraoperative Complications

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

Study Officials

  • Mingkwan Wongyingsinn

    Siriraj Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

June 15, 2022

First Posted

June 24, 2022

Study Start

July 1, 2022

Primary Completion (Estimated)

November 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

March 6, 2026

Record last verified: 2025-06

Locations