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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04021212
Other study ID # 20190712
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2020
Est. completion date June 2024

Study information

Verified date May 2022
Source Shandong Provincial Hospital
Contact Ling Gao
Phone +86 53168776910
Email linggao@sdu.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pituitary adenomas are usually benign monoclonal neoplasms caused by a mixture of pituicyte alterations together with a changed endocrine and paracrine regulatory milieu. Thus, it can cause serious health problems such as abnormal target organ function, pain, disability and even death. In clinical practice, we found many patients with pituitary adenomas are usually accompanied by hyperlipidemia, which is the main cause of cardiovascular diseases. However, it has been unclear if there is an association between pituitary adenomas and serum lipid profile. In the present study, we aim to focus on the patients with pituitary adenomas and their lipid profile before and after operation including first occurrence and recurrence.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: 1. Patients diagnosed with pituitary adenomas 2. All adenomas were resected by transsphenoidal surgery and identified by histological diagnoses. Exclusion Criteria: 1. Missing vital data, such as age, gender, serum lipid profile, pathology reports; 2. Complications or conditions that affect pituitary status and lipid metabolism, such as pregnancy, malignant adenomas or severe hepatic or renal dysfunction and 3. Use of any medication that affects the pituitary or lipid metabolism, including statins, fibrates, thyroid hormones, anti-thyroid drugs, iodine, amiodarone, alemtuzumab, lithium, tyrosine kinase inhibitors, interferon, estrogens, androgens,glucocorticoids, nonsteroidal anti-inflammatory drugs, antiepileptic drugs, rifampicin, furosemide, heparin or ß-adrenoceptor blockers in the past 3 months.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Shandong Provincial Hospital Jinan Shandong

Sponsors (1)

Lead Sponsor Collaborator
Shandong Provincial Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in serum lipid levels Measured at pre-operative and 6 months after operation