Insulin Resistance in Patients After Carotid Revascularization
Primary Purpose
Carotid Stenosis
Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Melatonin
blank
Sponsored by
About this trial
This is an interventional treatment trial for Carotid Stenosis focused on measuring carotid stenosis, melatonin, insulin resistance, inflammation, carotid revascularization, antioxidants
Eligibility Criteria
Inclusion Criteria:
- diagnosed with carotid stenosis
- had indications for carotid revascularization
Exclusion Criteria:
- surgical contraindication
- cardiovascular disease
- psychiatric disorders
- cancer
- pregnant
- lactating
- taking antipsychotic drugs during perioperative period
- history of trauma during perioperative period
Sites / Locations
- Peking Union Medical College HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Sham Comparator
Arm Label
surgery with melatonin
surgery with blank control
Arm Description
Patients under carotid revascularization surgery with melatonin taken during perioperative period.
Patients under carotid revascularization surgery with nothing unnecessary taken during perioperative period
Outcomes
Primary Outcome Measures
insulin resistance in patients under carotid revascularization assessed by the concentration of insulin
perioperative insulin resistance detected by the concentration of insulin by ELISA kit
inflammation in patients under carotid revascularization assessed by the concentration of IL-6
inflammation detected by the concentration of IL-6 by ELISA kit
inflammation in patients under carotid revascularization assessed by the concentration of TNF-ฮฑ
inflammation detected by the concentration of TNF-ฮฑ by ELISA kit
inflammation in patients under carotid revascularization assessed by the concentration of eNOS
inflammation detected by the concentration of eNOS by ELISA kit
oxidative stress in patients under carotid revascularization assessed by the concentration of CAT
oxidative stress detected by the concentration of CAT by ELISA kit
oxidative stress in patients under carotid revascularization assessed by the concentration of MDA
oxidative stress detected by the concentration of MDA by ELISA kit
oxidative stress in patients under carotid revascularization assessed by the concentration of SOD
oxidative stress detected by the concentration of SOD by ELISA kit
Secondary Outcome Measures
Full Information
NCT ID
NCT03419767
First Posted
January 27, 2018
Last Updated
January 27, 2018
Sponsor
Peking Union Medical College Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03419767
Brief Title
Insulin Resistance in Patients After Carotid Revascularization
Official Title
The Problem of Insulin Resistance in Patients After Carotid Revascularization
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2017 (Actual)
Primary Completion Date
June 1, 2018 (Anticipated)
Study Completion Date
June 1, 2018 (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
Data Monitoring Committee
No
5. Study Description
Brief Summary
The main purpose of this study is to study the phenomenon of insulin resistance in patients after carotid revascularization surgery through population-based, randomized, double-blind, placebo-controlled trial.
Detailed Description
Trial Title: Insulin Resistance in Patients After Carotid Revascularization. Protocol: Investigators recruited eligible Han Chinese participants (aged 40-80) who were diagnosed with carotid stenosis and had indications for carotid revascularization surgery. Participants were excluded if participants had undergone surgical contraindication, or psychiatric disorders, or cancer, or pregnant, or lactating, or taking antipsychotic drugs during perioperative period. Participants were randomly divided into groups of oral melatonin, and blank control. Participants in groups of oral melatonin took melatonin orally 6mg/day from 3 days before operation to 3 days after operation. Blood samples (about 6 milliliter) were taken at baseline, the first, the second, and the third morning after the operation, all in the fasting state. Through a series hospital clinical laboratory and related ELISA kits to detect the insulin, C-peptide and glucose in serum. Superoxide dismutase (SOD), malonaldehyde (MDA), catalase(CAT), endothelial nitric oxide synthase (eNOS), Interleukin 6 (IL-6), tumour necrosis factor(TNF-ฮฑ), were included for analysis to verify whether melatonin have protective effect for inflammation and oxidative stress in patients under carotid revascularization, which might be the mechanism of insulin resistance after surgery. This trial is approved by the Ethics Committee of Peking Union Medical College Hospital (No. ZS-1468). All participants completed a questionnaire and signed an informed consent document. Otherwise, participants will get appropriate economic compensation. Trial associates monitored compliance with the masking procedure throughout the trial. All participants and study investigators were unaware of treatment allocation throughout the study. The randomization codes remained sealed until after data collection and cleaning, and completion of a masked analysis. The study team monitored and classified protocol deviations. Investigators summarized baseline clinical and demographic characteristics with descriptive statistics and then determined by the Univariate Analysis of Variance. All the data analyses were done using statistical software SPSS 20.0.
Expected results: Postoperative levels of insulin resistance in both groups are higher than the preoperative. Compared with the blank control group, patients taking melatonin might have lower postoperative levels of insulin resistance, inflammation and oxidative stress.
Consent document: The potential risk, research as a treatment drug of melatonin may delay the metabolism of antipsychotic antipsychotic drug, so when investigators recruit psychiatric disorders or taking antipsychotic drugs orally during the 2 weeks of the trial should exclusion. As a Health care medicine, Melatonin is not suitable for children, so investigators selected recruiting participants under the age of 40 to 80.
The measure to minimize the risk, fully inform the participants and their families the trial's advantages, disadvantages and desired effect. All participants totally agree with the subjects. In this process, at least three or more effective way to get contact with the medical staff or doctor and ensure that those unexpected accident should deserve effective tackle. Participants guarantee to comply with the criterion before start of the trial. Our research involves the application of melatonin is through the china food and drug administration (CFDA) approved to ensure its safety (include its chemical composition, structure, content parameters, main raw material and appropriate crowd). All staff is qualified medical professionals to guarantee the safety of all participants.
The potential risks or discomfort, or inconvenience, or benefits for participants: So far, effective of melatonin in human include regulating sleep, anti-tumor, immune regulation, regulating of inflammation and immune and regulating blood lipid metabolism is confirmed. Adverse reactions is the delay of antipsychotic drug metabolism (so nearly one month ago and during period of the trial participants should not taking antipsychotic drugs) during the trial. The basic principle during the trial is ensure safety of participants.
The relevant content consultation: Everyone have the right to consultation the research content through telephone: +86 01069152500 (principal investigator) and +86 01069155817(Ethics committee).
The rights of withdrew from the trial: Participate in the trial is completely voluntary. If for any reason, participants not willing to participate in, or do not wish to continue to participate in this trial, will not affect the rights and interests of participants. In addition, participants have the right to withdraw this trial at any time. If participants do not accord to the doctor instructions, or for the sake of patients' health and benefits, the doctor or the researchers may also require participants to quit the trial.
The compensation of research: If the participants have any unexpected accident relation with the trial, the compensation and responsibility will be provided by Peking Union Medical College Hospital.
Privacy protection: The privacy of every participant will be protected. The results of the trial in academic publications will not leak any information to identify your personal identity. Peking Union Medical College Hospital will save everybody's data and guarantee not leak without authorization.
Investigators declare no competing interests.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carotid Stenosis
Keywords
carotid stenosis, melatonin, insulin resistance, inflammation, carotid revascularization, antioxidants
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
surgery with melatonin
Arm Type
Active Comparator
Arm Description
Patients under carotid revascularization surgery with melatonin taken during perioperative period.
Arm Title
surgery with blank control
Arm Type
Sham Comparator
Arm Description
Patients under carotid revascularization surgery with nothing unnecessary taken during perioperative period
Intervention Type
Drug
Intervention Name(s)
Melatonin
Intervention Description
Patients under carotid revascularization surgery taking 6mg/day melatonin orally from 3 days before operation to 3 days after operation.
Intervention Type
Other
Intervention Name(s)
blank
Intervention Description
Patients under carotid revascularization surgery without taking melatonin
Primary Outcome Measure Information:
Title
insulin resistance in patients under carotid revascularization assessed by the concentration of insulin
Description
perioperative insulin resistance detected by the concentration of insulin by ELISA kit
Time Frame
3 months
Title
inflammation in patients under carotid revascularization assessed by the concentration of IL-6
Description
inflammation detected by the concentration of IL-6 by ELISA kit
Time Frame
3 months
Title
inflammation in patients under carotid revascularization assessed by the concentration of TNF-ฮฑ
Description
inflammation detected by the concentration of TNF-ฮฑ by ELISA kit
Time Frame
3 months
Title
inflammation in patients under carotid revascularization assessed by the concentration of eNOS
Description
inflammation detected by the concentration of eNOS by ELISA kit
Time Frame
3 months
Title
oxidative stress in patients under carotid revascularization assessed by the concentration of CAT
Description
oxidative stress detected by the concentration of CAT by ELISA kit
Time Frame
3 months
Title
oxidative stress in patients under carotid revascularization assessed by the concentration of MDA
Description
oxidative stress detected by the concentration of MDA by ELISA kit
Time Frame
3 months
Title
oxidative stress in patients under carotid revascularization assessed by the concentration of SOD
Description
oxidative stress detected by the concentration of SOD by ELISA kit
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diagnosed with carotid stenosis
had indications for carotid revascularization
Exclusion Criteria:
surgical contraindication
cardiovascular disease
psychiatric disorders
cancer
pregnant
lactating
taking antipsychotic drugs during perioperative period
history of trauma during perioperative period
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Changwei Liu, MD
Phone
69152500
Email
liucw@vip.sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Changwei Liu, MD
Organizational Affiliation
Peking Union Medical College Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking Union Medical College Hospital
City
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Changwei Liu, MD
Phone
69152500
Email
liucw@vip.sina.com
First Name & Middle Initial & Last Name & Degree
Changwei Liu, MD
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Insulin Resistance in Patients After Carotid Revascularization
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