Craniopharyngioma With Tumoral Hemorrhage

Sponsor
Tongji Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04937335
Collaborator
(none)
185
97

Study Details

Study Description

Brief Summary

Clinical data of 185 consecutive patients receiving resective operation with a pathological diagnosis of craniopharyngioma in our hospital between January 2013 and February 2021 were collected. Among these patients, 18 of them were recognized as craniopharyngioma with tumoral hemorrhage during the operation.

Condition or Disease Intervention/Treatment Phase
  • Other: intratumoral hemorrhage

Detailed Description

For each case, age, gender, smoking status, alcohol intake, past history, symptoms, blood pressure, blood cell count, blood biochemical tests, coagulation tests, hormone tests, radiological results, surgical treatment and the outcome at discharge were collected. The first test result after admission and before the operation was taken for the items of blood tests with multiple times in the analysis.

Study Design

Study Type:
Observational
Actual Enrollment :
185 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Clinical Features and Risk Factors of Craniopharyngioma With Tumoral Hemorrhage
Actual Study Start Date :
Jan 1, 2013
Actual Primary Completion Date :
Feb 1, 2021
Actual Study Completion Date :
Feb 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Non-hemorrhage group

Patients recognized as craniopharyngioma pathologically without tumoral hemorrhage observed during the operation

Hemorrhage group

Patients recognized as craniopharyngioma pathologically with tumoral hemorrhage observed during the operation

Other: intratumoral hemorrhage
Patients who were recognized as craniopharyngioma pathologically with tumoral hemorrhage observed during the operation were enrolled in the hemorrhage group.

Outcome Measures

Primary Outcome Measures

  1. craniopharyngioma with tumoral hemorrhage [during the operation]

    Current study is a case-control study whose primary outcome is tumoral hemorrhage observed during the operation, which devided the craniopharyngioma patients into hemorrhage group and non-hemorrhage group.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • receive resective operation with a pathological diagnosis of craniopharyngioma in our hospital

  • enter our hospital between January 2013 and February 2021

Exclusion Criteria:
  • have a non-craniopharyngioma or unverified pathological diagnosis at discharge

  • have received surgical or radiological treatment on the sellar region

  • receive treatment of coagulation modulation, immunosuppressive agents or chemotherapeutic drugs

  • combine with other clinical emergencies including acute myocardial infarction, cerebral stroke, trauma and sepsis at admission

  • have been diagnosed with other tumors, hematological diseases, autoimmune diseases, liver failure or renal failure

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Tongji Hospital

Investigators

  • Study Director: Kai Shu, MD, Tongji Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Kai Shu, Prof. Dr., Tongji Hospital
ClinicalTrials.gov Identifier:
NCT04937335
Other Study ID Numbers:
  • kaishu1
First Posted:
Jun 24, 2021
Last Update Posted:
Jun 24, 2021
Last Verified:
Jun 1, 2021
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 Kai Shu, Prof. Dr., Tongji Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 24, 2021