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Restless Legs Syndrome in Hemodialysis Patients

Primary Purpose

Restless Leg Syndrome

Status
Completed
Phase
Not Applicable
Locations
Lebanon
Study Type
Interventional
Intervention
Vitamin C
Placebo
Sponsored by
Makassed General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Restless Leg Syndrome

Eligibility Criteria

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

Inclusion Criteria:

  • patients under regular hemodialysis
  • with no acute illness
  • not hospitalized

Exclusion Criteria:

  • Patients receiving:
  • tricyclic antidepressants,
  • selective serotonin reuptake inhibitors,
  • dopamine antagonists,
  • dopamine blocking,
  • antiemetics,
  • lithium,
  • sedative antihistamines,
  • Patients with a history of renal stones

Sites / Locations

  • Makassed General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Vitamin C

Placebo

Arm Description

RLS positive patients will be assessed for the severity. They will be given 200 mg Vitamin C for 8 weeks duration. Patients will be re-assessed for the severity of restless leg syndrome.

RLS positive patients will be assessed for the severity. They will be given 200 mg placebo for 8 weeks duration. Patients will be re-assessed for the severity of restless leg syndrome.

Outcomes

Primary Outcome Measures

change in the international restless legs syndrome (IRLS) rating scale score
change in the IRLS rating scale sum score from baseline to the end of treatment.The scale ranges between 0 and 40 which is the total score. A score between 31 and 40, indicates very severe RLS. A score between 21 and 30 indicates severe RLS. A score between 11 and 20 indicates moderate RLS. A score between 1 and 10 indicates mild RLS and a score of 0 means no RLS.

Secondary Outcome Measures

incidence of RLS
identify the incidence of restless legs syndrome in end stage renal disease (ESRD) patients on dialysis in Lebanon
Risk factors
identify risk factors associated with RLS

Full Information

First Posted
November 6, 2017
Last Updated
May 16, 2018
Sponsor
Makassed General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03337529
Brief Title
Restless Legs Syndrome in Hemodialysis Patients
Official Title
Restless Legs Syndrome in Hemodialysis Patients: Prevalence, Associated Risk Factors and Efficacy of Vitamin C as a Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
September 15, 2017 (Actual)
Primary Completion Date
April 15, 2018 (Actual)
Study Completion Date
April 15, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Makassed General 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
Restless legs syndrome (RLS) is defined as the spontaneous movement of the limbs (mainly legs) associated with unpleasant - painful sensation which is relieved by moving the affected limb. It is a common disorder in hemodialysis patients that leads to insomnia, impaired daytime functioning and quality of life. Symptoms of RLS are estimated to affect up to 25% of patients on dialysis when the international RLS diagnostic criteria are applied. Various pharmacological and non-pharmacological interventions have been used to treat primary RLS. However, the evidence for use of these interventions in people with End stage renal disease is not well established; and some have serious side effects. Because high oxidative stress has been implicated in the pathogenesis of RLS, investigators thought of evaluating the efficacy of vitamin C in reducing the severity of RLS symptoms in hemodialysis patients in this randomized, double-blind, placebo-controlled, two arm parallel trial. To note that only two studies were done worldwide that proved the efficacy of vitamin C in those patients.
Detailed Description
The investigators are proposing to carry out a clinical trial. Around 100 stable hemodialysis adult patients at Makassed general hospital dialysis center and around 150 patients at Sahel general hospital and Zahraa hospital will be assessed according to the international RLS criteria. The data on individual, clinical and laboratory indices will be obtained from patients' recorded files and interviews. The investigators will compare the RLS group versus the non RLS group according to these factors to find the independently associated factors for RLS in dialysis patients. Those who fulfill all four diagnostic criteria for RLS (confirmed independently by 2 neurologists) will be classified as "RLS positive" and will be asked to answer 10 questions on the international RLS study group (IRLSSG) rating scale. The IRLSSG rating scale was also used to evaluate the severity of RLS symptoms. These patients will be randomly allocated to two parallel groups to receive vitamin C (200 mg) or placebo for eight weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Restless Leg Syndrome

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin C
Arm Type
Experimental
Arm Description
RLS positive patients will be assessed for the severity. They will be given 200 mg Vitamin C for 8 weeks duration. Patients will be re-assessed for the severity of restless leg syndrome.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
RLS positive patients will be assessed for the severity. They will be given 200 mg placebo for 8 weeks duration. Patients will be re-assessed for the severity of restless leg syndrome.
Intervention Type
Other
Intervention Name(s)
Vitamin C
Intervention Description
200 mg Vitamin C will be given on daily basis for 8 weeks
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
200 mg placebo will be given on daily basis for 8 weeks
Primary Outcome Measure Information:
Title
change in the international restless legs syndrome (IRLS) rating scale score
Description
change in the IRLS rating scale sum score from baseline to the end of treatment.The scale ranges between 0 and 40 which is the total score. A score between 31 and 40, indicates very severe RLS. A score between 21 and 30 indicates severe RLS. A score between 11 and 20 indicates moderate RLS. A score between 1 and 10 indicates mild RLS and a score of 0 means no RLS.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
incidence of RLS
Description
identify the incidence of restless legs syndrome in end stage renal disease (ESRD) patients on dialysis in Lebanon
Time Frame
8 weeks
Title
Risk factors
Description
identify risk factors associated with RLS
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients under regular hemodialysis with no acute illness not hospitalized Exclusion Criteria: Patients receiving: tricyclic antidepressants, selective serotonin reuptake inhibitors, dopamine antagonists, dopamine blocking, antiemetics, lithium, sedative antihistamines, Patients with a history of renal stones
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hania Jarkas, MD
Organizational Affiliation
Makassed General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Makassed General Hospital
City
Beirut
Country
Lebanon

12. IPD Sharing Statement

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Restless Legs Syndrome in Hemodialysis Patients

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