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Hydrocortisone Use During Peri-operation for Pituitary Adenomas

Primary Purpose

Pituitary Adenoma, Adrenal Insufficiency, Surgery

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Normal saline
Hydrocortisone
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pituitary Adenoma focused on measuring Pituitary Adenomas, Peri-operation, Hydrocortisone, Adrenal Insufficiency

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with pituitary adenomas that need surgical resection of the tumor, whose hypothalamus-pituitary-adrenal axis are intact
  • Patients of either gender aged from 18 years to 70 years

Exclusion Criteria:

  • Patients with Cushing's disease
  • Patients with pituitary adenomas who have already developed secondary adrenal insufficiency before surgery
  • Patients with pituitary apoplexy or other acute pituitary conditions that need emergency surgery
  • The postoperative pathology result indicates that the tumor is not a pituitary adenoma
  • Patients that refuse to participate in the study or those who ask to quit after enrollment

Sites / Locations

  • Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Hydrocortisone withholding group

Hydrocortisone group

Arm Description

Patients receive no hydrocortisone

Patients receive routine hydrocortisone

Outcomes

Primary Outcome Measures

Rate of newly-onset adrenal insufficiency
Adrenal insufficiency: lower-than-normal serum cortisol level at 8 a.m., plus the following related symptoms, including serious fatigue, muscle weakness, decreased appetite, nausea, vomiting, diarrhea, low blood pressure, palpitation, and fever.

Secondary Outcome Measures

Rate of newly-onset adrenal insufficiency
Adrenal insufficiency: lower-than-normal serum cortisol level at 8 a.m., plus the following related symptoms, including serious fatigue, muscle weakness, decreased appetite, nausea, vomiting, diarrhea, low blood pressure, palpitation, and fever.

Full Information

First Posted
October 28, 2020
Last Updated
November 3, 2020
Sponsor
Peking Union Medical College Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04621565
Brief Title
Hydrocortisone Use During Peri-operation for Pituitary Adenomas
Official Title
Withholding Hydrocortisone vs Routine Use of Hydrocortisone During Peri-operation in Pituitary Adenoma Patients With Intact Hypothalamus-Pituitary-Adrenal Axis: Randomized Controlled Trial to Assess Safety and Complications
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2020 (Actual)
Primary Completion Date
July 2022 (Anticipated)
Study Completion Date
July 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking Union Medical College Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The investigators hypothesize that withholding hydrocortisone during the peri-operation in patients with pituitary adenomas whose hypothalamus pituitary adrenal axis are intact are safe.
Detailed Description
Pituitary is the headquarters of the endocrine system of the body, secreting several hormones maintaining the normal function of the endocrine organs. After surgery, pituitary dysfunction is seen in a small proportion of patients, even in some patients resulting in severe consequence, i.e. adrenal insufficiency or pituitary crisis. Therefore, patients undergoing pituitary surgery have been usually given "stress dose" steroids whether their hypothalamus pituitary adrenal (HPA) axis are deficient or preserved. Results of several retrospective studies showed that there was no significantly increase in postoperative adrenal insufficiency in no supplementation (of hydrocortisone) group than in supplementation group. Given the considerable side effects of using steroids, whether hydrocortisone administration is necessary for all patients with pituitary adenomas during peri-operation needs to be discussed. For Chinese patients with pituitary adenomas except for those of Cushing's disease, hydrocortisone administration during the peri-operation is a routine practice. Peking Union Medical College Hospital is the China Pituitary Disease Registry Center. Here, the investigators aim to launch a single-center prospective randomized controlled trial to verify the hypothesis that withholding hydrocortisone during the peri-operation in patients with pituitary adenomas whose HPA axis are intact are safe.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pituitary Adenoma, Adrenal Insufficiency, Surgery
Keywords
Pituitary Adenomas, Peri-operation, Hydrocortisone, Adrenal Insufficiency

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants are assigned to one of two groups, whether using hydrocortisone or not during peri-operation, in parallel for the duration of the study.
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
Participant, investigator, and outcome assessors are all prevented from having knowledge of the interventions assigned to individual participants. Care provider knows the individualized interventions.
Allocation
Randomized
Enrollment
436 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Hydrocortisone withholding group
Arm Type
Experimental
Arm Description
Patients receive no hydrocortisone
Arm Title
Hydrocortisone group
Arm Type
Active Comparator
Arm Description
Patients receive routine hydrocortisone
Intervention Type
Drug
Intervention Name(s)
Normal saline
Other Intervention Name(s)
Intravenous normal saline
Intervention Description
No hydrocortisone or other steroids are given before, during, and after the surgery, except that patients develop postoperative adrenal insufficiency. If a patient develops postoperative adrenal insufficiency, he/she needs to receive hydrocortisone treatment (20mg at 0800 and 20mg at 1600) for one month and then check the level of morning serum cortisol to decide if it is time to start the hydrocortisone taper program.
Intervention Type
Drug
Intervention Name(s)
Hydrocortisone
Other Intervention Name(s)
Hydrocortisone sodium succinate (iv.) & Hydrocortisone (po.)
Intervention Description
Hydrocortisone sodium succinate is given on the operation day (100mg at 0800 & 100mg at 2000), the postoperative day 1 (100mg at 0800 & 50mg at 2000), and the postoperative day 2 (25mg at 0800). Hydrocortisone (po.) is then given starting from the afternoon of postoperative day 2 (20mg at 1600 and 0800) to the end of the first postoperative week, and 20mg at 0800 during the second postoperative week. This is called the "hydrocortisone taper program". If a patient develops postoperative adrenal insufficiency, he/she needs to receive hydrocortisone treatment (20mg at 0800 and 20mg at 1600) for one month and then check the level of morning serum cortisol to decide if it is time to start the hydrocortisone taper program.
Primary Outcome Measure Information:
Title
Rate of newly-onset adrenal insufficiency
Description
Adrenal insufficiency: lower-than-normal serum cortisol level at 8 a.m., plus the following related symptoms, including serious fatigue, muscle weakness, decreased appetite, nausea, vomiting, diarrhea, low blood pressure, palpitation, and fever.
Time Frame
During the first 3 postoperative days
Secondary Outcome Measure Information:
Title
Rate of newly-onset adrenal insufficiency
Description
Adrenal insufficiency: lower-than-normal serum cortisol level at 8 a.m., plus the following related symptoms, including serious fatigue, muscle weakness, decreased appetite, nausea, vomiting, diarrhea, low blood pressure, palpitation, and fever.
Time Frame
From the 3rd postoperative day to the 3rd postoperative month
Other Pre-specified Outcome Measures:
Title
Rate of newly-developed diabetes mellitus
Description
A random reading of blood sugar level more than 200 mg/dL (11.1 mmol/L), or a reading after two hours (after OGTT) over 200 mg/dL (11.1 mmol/L) indicates diabetes mellitus.
Time Frame
During the first 3 postoperative months
Title
Rate of newly-developed diabetes insipidus
Description
Urine volume > 300ml for more than 3h or > 6 liter per day, specific gravity of urine <1.003, and serum sodium levels > 145 mmol/L indicate diabetes insipidus.
Time Frame
During the first 3 postoperative months
Title
Concentration of blood electrolytes
Description
The level of Na+, K+, and Ca++ in the blood
Time Frame
At the 3rd postoperative month
Title
Concentration of blood cells
Description
Numbers of erythrocytes, leukocytes, neutrophils, lymphocytes, thrombocytes in the blood
Time Frame
At the 3rd postoperative month
Title
Percentage of blood cells
Description
Percentage of neutrophils, monocytes, lymphocytes of the leukocytes
Time Frame
At the 3rd postoperative month
Title
Concentration of indexes of coagulation function #1
Description
Prothrombin time, activated partial thromboplastin time, and thrombin time
Time Frame
At the 3rd postoperative month
Title
Level of international normalized ratio
Description
Level of international normalized ratio
Time Frame
At the 3rd postoperative month
Title
Level of D-Dimer
Description
Level of D-Dimer
Time Frame
At the 3rd postoperative month
Title
Rate of deep venous thrombosis
Description
Deep venous thrombosis as detected by ultrasound
Time Frame
During the first 3 postoperative months
Title
Rate of other complications
Description
Decreased bone density, osteoporosis, fracture, acne, and infections.
Time Frame
During the first 3 postoperative months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with pituitary adenomas that need surgical resection of the tumor, whose hypothalamus-pituitary-adrenal axis are intact Patients of either gender aged from 18 years to 70 years Exclusion Criteria: Patients with Cushing's disease Patients with pituitary adenomas who have already developed secondary adrenal insufficiency before surgery Patients with pituitary apoplexy or other acute pituitary conditions that need emergency surgery The postoperative pathology result indicates that the tumor is not a pituitary adenoma Patients that refuse to participate in the study or those who ask to quit after enrollment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bing Xing, MD
Phone
+861069152530
Email
xingbingemail@aliyun.com
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaopeng Guo, MD
Phone
+8617701220936
Email
guoxiaopeng_pumch@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bing Xing, MD
Organizational Affiliation
Neurosurgery, Peking Union Medical College Hospital, Beijing, China
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Wei Lian, MD
Organizational Affiliation
Neurosurgery, Peking Union Medical College Hospital, Beijing, China
Official's Role
Study Director
Facility Information:
Facility Name
Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bing Xing, MD
Phone
+861069152530
Email
xingbingemail@aliyun.com
First Name & Middle Initial & Last Name & Degree
Xiaopeng Guo, MD
Phone
+8617701220936
Email
guoxiaopeng_pumch@163.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
The individual participant data will be available upon reasonable requests to the study chair, Dr. Bing Xing, or the study director, Dr. Wei Lian.
Citations:
PubMed Identifier
25775019
Citation
Tohti M, Li J, Zhou Y, Hu Y, Yu Z, Ma C. Is peri-operative steroid replacement therapy necessary for the pituitary adenomas treated with surgery? A systematic review and meta analysis. PLoS One. 2015 Mar 16;10(3):e0119621. doi: 10.1371/journal.pone.0119621. eCollection 2015.
Results Reference
background
PubMed Identifier
30325449
Citation
Sterl K, Thompson B, Goss CW, Dacey RG, Rich KM, Zipfel GJ, Chicoine MR, Kim AH, Silverstein JM. Withholding Perioperative Steroids in Patients Undergoing Transsphenoidal Resection for Pituitary Disease: Randomized Prospective Clinical Trial to Assess Safety. Neurosurgery. 2019 Aug 1;85(2):E226-E232. doi: 10.1093/neuros/nyy479.
Results Reference
background
PubMed Identifier
31978882
Citation
Lee HC, Yoon HK, Kim JH, Kim YH, Park HP. Comparison of intraoperative cortisol levels after preoperative hydrocortisone administration versus placebo in patients without adrenal insufficiency undergoing endoscopic transsphenoidal removal of nonfunctioning pituitary adenomas: a double-blind randomized trial. J Neurosurg. 2020 Jan 24;134(2):526-534. doi: 10.3171/2019.11.JNS192381.
Results Reference
background
PubMed Identifier
36383383
Citation
Guo X, Zhang D, Pang H, Wang Z, Gao L, Wang Y, Ma W, Lian W, Xing B; ZS-2608 Trial Team. Safety of Withholding Perioperative Hydrocortisone for Patients With Pituitary Adenomas With an Intact Hypothalamus-Pituitary-Adrenal Axis: A Randomized Clinical Trial. JAMA Netw Open. 2022 Nov 1;5(11):e2242221. doi: 10.1001/jamanetworkopen.2022.42221.
Results Reference
derived

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Hydrocortisone Use During Peri-operation for Pituitary Adenomas

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