Exploring the Impact of Diurnal Variation on Coagulation Function in Patients Undering Tumor Surgery
1 other identifier
observational
60
1 country
1
Brief Summary
Studies have shown that compared to the evening, the platelet adhension and aggregation functions of normal individuals are stronger in the morning, reaching peak at around 8AM or 9AM. Fibrinolysis is weakest at 7-11AM, and most active at midnight. previous studies have been contradictory regarding the rhythm of plasmin. Some show the level of plasmin complexes is highest at night, while some show higher in the morning and some show there is no rhythmicity. Since patients with tumors often have a hypercoagulable state, we try to find a method to assess whether cancer patients have the same circadian with heathy individuals. And whether the surgery time(in the morning or in the evening) will affect the tumor patients' postoperative coagulation function
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jun 2025
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2025
CompletedFirst Submitted
Initial submission to the registry
September 20, 2026
CompletedFirst Posted
Study publicly available on registry
September 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 30, 2027
September 25, 2026
May 1, 2026
1.6 years
September 20, 2026
September 20, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
preoperative TEG values
one day
Study Arms (2)
morning surgery group
night surgery group
Interventions
Eligibility Criteria
The subjects of the study were 83 patients scheduled for gastrointestinal tumor surgery under general anesthesia.
You may qualify if:
- \) Patients who signed the informed consent form and were willing to complete the study according to the protocol.
- \) Patients who underwent surgical treatment for digestive tract tumors. 3) The operation start time was from 8:00 to 9:00 in the morning and from 19:00 to 20:00 in the evening.
- \) ASA grade I-II. 5) Age ranging from 20 to 70 years old.
You may not qualify if:
- \) History of thrombosis-related diseases 2) Use of anticoagulants (excluding aspirin, which should be discontinued for one week) 3) Hb \< 90g/dL 4) Diabetic patients \[14\] 5) Patients admitted to ICU after surgery 10) Those who have participated in other clinical trials or refused to join the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Fudan Universitylead
Study Sites (1)
Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, 200333, China
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- chief of anesthesia at Fudan University Cancer Center
Study Record Dates
First Submitted
September 20, 2026
First Posted
September 25, 2026
Study Start
June 1, 2025
Primary Completion (Estimated)
December 30, 2026
Study Completion (Estimated)
July 30, 2027
Last Updated
September 25, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share