Pituitary Adenoma Clinical Trial
— TRANSSPHEROfficial title:
Prospective Multicenter Cohort Study Comparing Extent of Tumor Resection Between Microscopic Transsphenoidal Surgery and Fully Endoscopic Transsphenoidal Surgery for Nonfunctioning Pituitary Adenomas
NCT number | NCT02357498 |
Other study ID # | 14BN151 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | February 1, 2015 |
Est. completion date | April 8, 2019 |
Verified date | November 2019 |
Source | St. Joseph's Hospital and Medical Center, Phoenix |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this research study is to compare the extent of resection (EOR) in patients with nonfunctioning pituitary adenomas undergoing transsphenoidal surgery using a microsurgical technique to those patients who have undergone surgery with a fully endoscopic technique. Another goal is to compare surgical complications, endocrine outcomes, visual outcomes, length of surgery, length of hospital stay, and readmission rates between the two transsphenoidal surgery techniques. This is an observational data collection study with no experimental procedures or experimental medicines. Endonasal transsphenoidal removal of a pituitary tumor is a unique procedure and there is little information comparing the two surgical techniques.
Status | Completed |
Enrollment | 260 |
Est. completion date | April 8, 2019 |
Est. primary completion date | February 1, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Patients with suspected nonfunctioning pituitary macroadenomas (= 1 cm) with planned transsphenoidal surgery - Adults (age 18-80 years) - Medically stable for surgery - Reasonable expectation that patient will complete study and be available for follow-up assessments Exclusion Criteria: - Prisoners - Pregnant women - Patients with suspected functioning pituitary adenoma - Unable to obtain MRI of the pituitary (e.g., pacemaker, anaphylaxis to gadolinium, low GFR) - Pituitary apoplexy |
Country | Name | City | State |
---|---|---|---|
United States | Northwestern University | Chicago | Illinois |
United States | Ohio State University Medical Center | Columbus | Ohio |
United States | Ronald Reagan UCLA Medical Center | Los Angeles | California |
United States | Barrow Neurological Institute/St. Joseph's Hospital and Medical Center | Phoenix | Arizona |
United States | Washington University School of Medicine | Saint Louis | Missouri |
United States | John Wayne Cancer Institute | Santa Monica | California |
United States | Swedish Neuroscience Institute | Seattle | Washington |
Lead Sponsor | Collaborator |
---|---|
St. Joseph's Hospital and Medical Center, Phoenix | John Wayne Cancer Institute, Northwestern University, Ohio State University, Swedish Medical Center, University of Pittsburgh Medical Center, Washington University School of Medicine |
United States,
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* Note: There are 26 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | percentage of patients who have complete tumor removal (gross total resection) based on MRI . | Postop MRI read by neuroradiologist | 3 months post surgery | |
Secondary | volume of residual tumor | volume, analyzed as a continuous variable; will be determined by manual segmentation using Dominator (www.dominator.com) software under the supervision of a board-certified neuroradiologist | 3 months after date of surgery | |
Secondary | percentage of tumor removed | Postop MRI tumor bed read by neuroradilogisy | 3 months post surgery | |
Secondary | postoperative cerebral-spinal fluid (CSF) leak | leakage from nose is a known complication, however, patients who have undergone a second surgery or had a lumbar drain placed to repair the problem will be documented | 6 months (continuous) from surgery | |
Secondary | postoperative meningitis | Determined by symptoms of headache, fever, neck stiffness, nausea and vomiting, and occasionally an altered level of consciousness. CSF culture may be positive for infection and may show elevated glucose and/or protein. CSF may be negative in aseptic meningitis. | 6 months (continuous) from surgery | |
Secondary | hypopituitarism | (morning cortisol <4.0ug/dL)(adrenocorticotropic hormone ACTH <6.0pg/mL)(follicular stimulating hormone FSH - mIU/mL. Female: follicular: <3.5; midcycle <4.7; luteal <1.7; postmenopausal <25.8. male <1.7)(luteinizing hormone LH - mIU/mL. Female: follicular <2.4; midcycle <14.0; luteal <1.0; postmenopausal <7.7)(estradiol - pg/mL. female: follicular <13; ovulation <86; luteal <44; postmenopausal <56)(insulin-like growth factor 1 IGF1: 101ng/mL)(testosterone total - ng/dL. Female <6.0; male <270.0)(prolactin ,3.3ng/mL)(thyroid stimulating hormone TSH <.45mU/L)(Thyroxine T4 Free <0.8ng/dL | 6 months post surgery | |
Secondary | diabetes insipidus (DI) | to be evaluated by pituitary endocrinologist; serum sodium value is > or equal to 147meq/dl OR if the patient received treatment for DI | 6 months post surgery | |
Secondary | visual outcomes | visual field deficits in this exam will be compared to pre-operative results. Confrontation visual field exam (Donder's test): The examiner will ask the patient to cover one eye and stare at the examiner. The examiner will then move his hand out of the patient's visual field and bring it back in. The examiner will use a slowly wagging finger or a hat pin for this. The patient signals the examiner when his hand comes back into view. Second option is a formal visual field exam (perimetry) performed by a neuro-ophthalmologist. | 3 months post surgery | |
Secondary | hypothyroidism | (thyroid stimulating hormone TSH <.45mU/L)(thyroxine T4Free <0.8ng/dL) | 6 months post surgery | |
Secondary | hypogonadism | (Testosterone (Total) - ng/dL. Female: < 6.0; Male: < 270.0) (Follicular Stimulating Hormone (FSH) - mIU/mL. Female - Follicular: < 3.5; Midcycle: <4.7; Luteal: < 1.7; Postmenopausal: < 25.8. Male - < 1.5)(Luteinizing Hormone LH - mIU/mL. Female: Follicular: < 2.4; Midcycle: <14.0; Luteal: < 1.0; Postmenopausal: < 7.7. Male: < 1.7)(Estradiol - pg/mL. Female: Follicular: < 13; Ovulation: < 86; Luteal: < 44; Postmenopausal: < 56. Male: < 15) | 6 months post surgery | |
Secondary | growth hormone deficiency | (insulin tolerance test: growth hormone <3µg/l)(IGF1 <77)(symptoms may include thin and dry skin, low energy, decreased strength and exercise tolerance, decreased muscle mass, weight gain especially around the waist, feelings of anxiety, depression, or sadness causing a change in social behavior | 6 months post surgery | |
Secondary | adrenal insufficiency | (morning serum cortisol <4.0ug/dL)(ACTH <6.0pg/mL)(sodium <135mEq/L)(abnormal ACTH [cosyntropin] stimulation test) | 6 months post surgery |
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