GCTHCM: Application of a New Type of Whole Blood Coagulation Time Measurement in Evaluating the Hypercoagulable State of Malignant Tumors

Sponsor
Tianjin Medical University General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05939960
Collaborator
(none)
354
1
15
23.6

Study Details

Study Description

Brief Summary

Malignant tumors are closely related to deep vein thrombosis, Pulmonary embolism and other diseases. Tumor patients usually have a hypercoagulable state (HCS) in their blood, and the proportion of thrombosis caused by HCS is more than 10 times that of non tumor patients. Conventional clinical testing methods such as coagulation function, blood routine, and thromboelastography are difficult to directly evaluate the hypercoagulable state of tumor patients. In addition, the widely used Khorana score and Caprini score systems in clinical practice need to be improved in accurately reflecting the hypercoagulable state of tumor patients.

Our team has established a complete new coagulation time measurement system, including general clotting time (GCT), platelet rich plasma clotting time (PRP-CT), and platelet poor plasma clotting time (PPP-CT), which may be a new and accurate method for evaluating tumor hypercoagulability.

The GCT study aims to evaluate: 1. The time of GCT, PRP-CT, and PPP-CT for malignant tumors is shorter than that of normal individuals, and some patients are in a hypercoagulable state; 2. The shortened time of GCT, PRP-CT, and PPP-CT may be associated with future thrombosis; 3. Evaluating the relationship between shortened GCT system time and overall tumor survival

Therefore, the GCT system evaluation may identify patients who are truly in a hypercoagulable state, providing monitoring indicators for subsequent anticoagulation; It can also be evaluated whether GCT time can reflect the prognosis of tumor patients.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: CGT test

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
354 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Application of a New Type of Whole Blood Coagulation Time Measurement in Evaluating the Hypercoagulable State of Malignant Tumors
Actual Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Feb 28, 2024
Anticipated Study Completion Date :
Sep 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Normal group

GCT time within normal range;Normal coagulation function

Diagnostic Test: CGT test
GCT、PRP-CT、PPP-CT monitor

hypercoagulable group

GCT time reduction; Normal coagulation function,

Diagnostic Test: CGT test
GCT、PRP-CT、PPP-CT monitor

Outcome Measures

Primary Outcome Measures

  1. Compared with non tumor patients, the GCT time of tumor patients is significantly GCT shortened in neoplames [July 1,2023 to September 30,2024]

    Compared with non tumor patients, the GCT time of tumor patients is significantly shortened

Secondary Outcome Measures

  1. theincreased incidence of VTE [July 1,2023 to September 30,2024]

    In patients with shortened GCT, the incidence of VTE increases.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Voluntarily participate and sign an informed consent form;

  2. Age ≥ 18 years old

  3. Expected survival time>6 months;

  4. Patients diagnosed with malignant tumors for the first time or progressing during treatment;

  5. Solid malignant tumors with clear pathological diagnosis;

  6. ECOG physical fitness score ≤ 2 points

Exclusion Criteria:
  1. Patients with known venous thrombosis (including upper and lower limb venous thrombosis, Pulmonary embolism, visceral venous thrombosis, etc.);

  2. Patients who have received long-term treatment with Warfarin, Rivaroxaban, and low-molecular-weight heparin (except aspirin, hydrogen Clopidogrel, etc.);

  3. Patients with active infections and sepsis;

  4. Hematology tumor (except lymphoma);

  5. Patients who undergo any major surgical treatment within 28 days prior to enrollment;

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tianjin Medical University General Hospital Tianjin Tianjin China 300170

Sponsors and Collaborators

  • Tianjin Medical University General Hospital

Investigators

  • Principal Investigator: Zhang Jianning, Doctor, Tianjin Medical University General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Qiong Qin, Director of Oncology Department, Tianjin Medical University General Hospital
ClinicalTrials.gov Identifier:
NCT05939960
Other Study ID Numbers:
  • IRB2023-RTFL-134
First Posted:
Jul 11, 2023
Last Update Posted:
Jul 11, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Qiong Qin, Director of Oncology Department, Tianjin Medical University General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 11, 2023