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Study on the surgical safety and treatment outcome of TSH tumor by using somatostatin analogue before surgery

Study on the surgical safety and treatment outcome of TSH tumor by using somatostatin analogue before surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030523
Enrollment
Unknown
Registered
2020-03-06
Start date
2020-03-20
Completion date
Unknown
Last updated
2020-03-09

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

Conditions

Thyroid stimulating hormone secreting pituitary adenoma

Interventions

experimental group:Octreotide injection 0.1mg q8h
control group:no Octreotide injection

Sponsors

Department of Endocrinology, Xinqiao Hospital, the Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. All the diagnostic criteria for TSH tumor included in the study are the diagnostic criteria recommended by Chinese experts in the diagnosis and treatment of pituitary thyrotropic hormone adenoma (2017) and ETA in 2013: (1) serum FT4 and FT3 are higher than the normal range, and the serum TSH level is not inhibited; (2) functional test: octreotide test suggested that it could be inhibited; (3) genetic testing: thyroxine receptor beta gene mutation detection suggested no exact significance of the mutation;(4) MRI plain scan and enhancement in the saddle region suggested pituitary adenoma. 2. Aged 18-70 years; 3. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe infection, trauma, surgery, heart failure, acute myocardial infarction, hypotension, hypoxia and other stress conditions; 2. Serious cardiovascular diseases, untreated hypertension and pulmonary insufficiency; 3. Participated in clinical trials of other drugs within 30 days; 4. The participant cannot participate in completing the intervention under other circumstances; 5. The researcher considers that the subjects have diseases that affect the outcome assessment or are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
thyroid hormones;MRI scan + enhancement in saddle region;Growth hormone and related hormones;Preoperative armour power control efficiency;Perioperative mortality;The incidence of perioperative hyperthyroidism crisis;

Secondary

MeasureTime frame
Sex hormones;Thyrotropin receptor artibody;Thyroid ultrasound;anesthetic accident;intraoperative blood loss;Duration of operation;intraoperative blood loss;surgical complication;Time of admission to icu after surgery;

Countries

China

Contacts

Public ContactLong Min

Department of Endocrinology, Translational Research Key Laboratory for Diabetes, Xinqiao Hospital, the Third Military Medical University

Longmin_casper@163.com+86 13640599383

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026