NCT07841613

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

75
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
10mo left

Started Jun 2025

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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 Progress62%
Jun 2025Jul 2027

Study Start

First participant enrolled

June 1, 2025

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

September 20, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 25, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2026

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2027

Last Updated

September 25, 2026

Status Verified

May 1, 2026

Enrollment Period

1.6 years

First QC Date

September 20, 2026

Last Update Submit

September 20, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • preoperative TEG values

    one day

Study Arms (2)

morning surgery group

night surgery group

Other: No Biologics

Interventions

no intervention

night surgery group

Eligibility Criteria

Age20 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Fudan University Shanghai Cancer Center

Shanghai, Shanghai Municipality, 200333, China

Location

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

Locations