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Predictors and Outcomes of Dysglycemia in Pheochromocytoma and Paraganglioma

Predictors and Outcomes of Dysglycemia in Pheochromocytoma and Paraganglioma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05451134
Enrollment
300
Registered
2022-07-11
Start date
2022-06-30
Completion date
2022-07-20
Last updated
2022-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pheochromocytoma, Paraganglioma

Keywords

Pheochromocytoma, Paraganglioma, dysglycemia

Brief 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.

Detailed 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.

Interventions

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

Sponsors

Peking Union Medical College Hospital
CollaboratorOTHER
China National Center for Cardiovascular Diseases
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline OGTT(oral glucose tolerance test)results to 6-12 months after surgeryBaseline, 6-12 months after surgeryOGTT 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

Secondary

MeasureTime frameDescription
random blood glucose resultsbaseline, 6-12 months after surgeryrandom blood glucose results at baseline and 6-12 months after surgery will be recorded to assess the effect of surgery on dysglycemia
HbA1cbaseline, 6-12 months after surgeryHbA1c results at baseline and 6-12 months after surgery will be recorded to assess the effect of surgery on dysglycemia
fasting blood glucosebaseline, 6-12 months after surgeryfasting blood glucose results at baseline and 6-12 months after surgery will be recorded to assess the effect of surgery on dysglycemia

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026