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China Treatment Trial for Tumor in Sellar Region With Unruptured Intracranial Aneurysm

Treatment Strategies for Tumor in Sellar Region With Unruptured Intracranial Aneurysms in the Chinese Population

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07809178
Acronym
ChTTSRUIA
Enrollment
608
Registered
2026-09-09
Start date
2026-09-01
Completion date
2031-09-01
Last updated
2026-09-09

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

Conditions

Chordoma, Craniopharyngioma, Germinoma, Hypothalamic Neoplasms, Meningioma, Optic Pathway Glioma, Pituitary Neuroendocrine Tumor, Rathke Cleft Cysts, Unruptured Intracranial Aneurysms

Keywords

Tumor in sellar region, Unruptured intracranial aneurysms

Brief summary

The goal of this observational study is to learn about the treatment strategies for tumor in sellar region with unruptured intracranial aneurysms in the Chinese population. The main question it aims to answer is: For patients with tumor in sellar region combined with unruptured intracranial aneurysms, which condition should be treated first?

Detailed description

The goal of this observational study is to clarify the treatment strategies for tumor in sellar region with unruptured intracranial aneurysms in the Chinese population aged from 18 to 75. The main question it aims to answer is: * What is the appropriate treatment strategy for patients diagnosed with tumor in sellar region with unruptured intracranial aneurysms? * Should the tumor be resected first followed by aneurysm treatment, or should the aneurysm be treated prior to tumor resection? Alternatively, is tumor resection alone with regular observation of the aneurysm a viable option? * What are the patient's intraoperative risks, postoperative complications, and prognosis? Participants are required to: * Provide detailed medical records. * Complete laboratory tests and imaging examinations at scheduled time points and cooperate with neurosurgeons for follow-up visits after the relevant treatments. This is an observational study. It solely collects patients' pre-operative, intra-operative, and post-operative follow-up information and does not influence the patient's treatment process or clinical decision-making.

Interventions

PROCEDURETumor resection followed by aneurysm treatment

Tumor resection followed by aneurysm treatment

PROCEDUREAneurysm treatment followed by tumor resection

Aneurysm treatment followed by tumor resection

OTHERObservation

Tumor resection without aneurysm treatment but observation

Sponsors

Cheng sen
Lead SponsorOTHER
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
CollaboratorOTHER
West China Hospital
CollaboratorOTHER
Xijing Hospital
CollaboratorOTHER
Shandong Provincial Hospital
CollaboratorOTHER_GOV
The First Affiliated Hospital of Anhui Medical University
CollaboratorOTHER
First Affiliated Hospital of Chongqing Medical University
CollaboratorOTHER
Shengjing Hospital
CollaboratorOTHER
Lanzhou University Second Hospital
CollaboratorOTHER
The First Hospital of Jilin University
CollaboratorOTHER
People's Hospital of Xinjiang Uygur Autonomous Region
CollaboratorOTHER
Guangdong Provincial Hospital of Traditional Chinese Medicine
CollaboratorOTHER
Huashan Hospital
CollaboratorOTHER
Jinling Hospital, China
CollaboratorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Preoperative enhanced head MRI showing a suspected diagnosis of a sella region lesion, and preoperative head CTA/DSA confirming an unruptured intracranial aneurysm. 2. Patients with primary sella region tumor and unruptured intracranial aneurysms that have not previously accepted surgical treatment. 3. Patients with tumor in sellar region requiring craniotomy or endoscopic transnasal surgery and/or an aneurysm requiring craniotomy, endovascular treatment, or observation only. 4. The patients are in good general health, without severe underlying medical conditions, and capable of tolerating surgical treatment. 5. Patients or their legal guardians have signed an informed consent form and voluntarily agreed to participate in the clinical trial.

Exclusion criteria

1. Patients with recurrent sella region tumors. 2. Patients with previously treated intracranial aneurysm. 3. Pregnant or breastfeeding women. 4. Any other condition that, in the investigator's judgment, makes the patient unsuitable for trial participation.

Design outcomes

Primary

MeasureTime frameDescription
Aneurysm progressionFrom enrollment to the end of treatment at 24 monthsThe diameter of aneurysm neck, the diameter of aneurysm dome, the volume of aneurysm, aneurysm rupture status
Tumor related complication and progressionFrom enrollment to the end of treatment at 24 monthsThe related complication and progression of tumor in sellar region: pituitary hormone level, visual acuity and visual field, hydrocephalus and tumor recurrence.

Countries

China

Contacts

CONTACTSen Cheng, MD
dr.sencheng@hotmail.com+8615313520109

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 10, 2026