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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05451134
Other study ID # 2022-06
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date June 30, 2022
Est. completion date July 20, 2022

Study information

Verified date June 2022
Source China National Center for Cardiovascular Diseases
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators will retrospectively analyze the clinical data of consecutive patients with pheochromocytomas and paragangliomas admitted between January 2018 and June 2020. The clinical characteristics of patients with and without dysglycemia will be compared, and whether surgery could improve the patients'dysglycemia will be also investigated.


Description:

This retrospective cohort study will include all consecutive adult patients who underwent surgery for PHEOs and catecholamine-secreting PGLs from January 2018 to June 2020. Patients with recurrent PPGLs, those who required steroids after adrenalectomy, and those with inadequate clinical records were excluded. The patients' electronic medical files were reviewed. Patients with dysglycemia included those with diabetes, or impaired fasting glucose, or impaired glucose tolerance. Clinical history data such as age, sex, body mass index (BMI), the presence of preoperative symptoms, biochemical test results, and tumor characteristics, such as tumor diameters and locations were extracted and analyzed.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 300
Est. completion date July 20, 2022
Est. primary completion date July 20, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - age =18 years old - patients with surgical pathological diagnosis of pheochromocytomas and paragangliomas(PPGLs) Exclusion Criteria: - recurrent PPGLs - patients who required steroids after adrenalectomy - patients with inadequate clinical records were excluded.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Catecholamines
Focus on whether catecholamine exposure is associated with dysglycemia in patients with pheochromocytoma and paraganglioma

Locations

Country Name City State
China Xian-Liang Zhou Beijing Beijing

Sponsors (2)

Lead Sponsor Collaborator
China National Center for Cardiovascular Diseases Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline OGTT(oral glucose tolerance test)results to 6-12 months after surgery OGTT results (including fasting blood glucose in the text, blood glucose results at 2 hours after oral administration of 75g glucose)at baseline and 6-12 months after surgery will be recorded to assess the effect of surgery on dysglycemia Baseline, 6-12 months after surgery
Secondary random blood glucose results random blood glucose results at baseline and 6-12 months after surgery will be recorded to assess the effect of surgery on dysglycemia baseline, 6-12 months after surgery
Secondary HbA1c HbA1c results at baseline and 6-12 months after surgery will be recorded to assess the effect of surgery on dysglycemia baseline, 6-12 months after surgery
Secondary fasting blood glucose fasting blood glucose results at baseline and 6-12 months after surgery will be recorded to assess the effect of surgery on dysglycemia baseline, 6-12 months after surgery
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