Skip to main content
Clinical Trials/ACTRN12610000741088
ACTRN12610000741088
Completed
Phase 3

A randomized controlled clinical trial comparing the efficacy of Dead Sea mineral enriched body lotion vs. two types of placebo in the treatment of cutaneous dryness, itching, peeling and tightness in hemodialysis patients: EDIT

Ahava Dead Sea Laboratories and Dead Sea Research Center0 sites75 target enrollmentSeptember 6, 2010

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Skin - Dermatological conditions
Sponsor
Ahava Dead Sea Laboratories and Dead Sea Research Center
Enrollment
75
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 6, 2010
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Ahava Dead Sea Laboratories and Dead Sea Research Center

Eligibility Criteria

Inclusion Criteria

  • Hemodialysis (HD) patients aged 40\-80 years inclusive were eligible for study participation if they received HD treatment three times each week for not less than three months, and if they were willing to refrain from any antipruritic treatment, oral or topical, for a period of not less than two weeks prior to study initiation. Patients of both genders, without regard to comorbidities or prescribed medications, were eligible.

Exclusion Criteria

  • Patient unwillingness to participate for any reason; known sensitivity to any of the ingredients in the active or placebo treatments.

Outcomes

Primary Outcomes

Not specified

Similar Trials

Completed
Not Applicable
Decapeptid effect in myomaMyoma.MyomaM8895/0
IRCT201012045307N1Vice Chancellor for Research, Hamedan University of Medical Sciences20
Recruiting
Not Applicable
A randomized controlled clinical trial comparing small buccal dehiscence defects around dental implants treated with an autogenous connective tissue graft (SCTG) or with standard guided bone regeneration (GBR).Missing tooth in the posterior area (premolar or molar)
DRKS00015194niversität Zürich, Zentrum für Zahnmedizin, Klinik für Rekonstruktive Zahnmedizin10
Recruiting
Phase 4
The efficacy of using Platelet-Rich Fibrin (PRF) with conventional technique of Cleft Palate RepairHealth Condition 1: Q359- Cleft palate, unspecified
CTRI/2024/07/071184Kahers Jawaharlal Nehru Medical College
Completed
Not Applicable
A study done in patients who have undergone diagnostic cardiac catheterization that determines the influence of two different positions- elevating the head end of bed and lying down straight on bed during the post procedure period, on patient perception of back pain and bleeding complications.Health Condition 1: null- Incidence and intensity of Back painVascular access-site complications(bleeding, hematoma, pseudo aneurysm)
CTRI/2011/06/001791All India Institute of Medical Sciences New Delhi80
Not yet recruiting
Not Applicable
A Randomised Controlled Clinical Trial comparing the results of the Immediate Loading (within 48 hours) of Mandibular Overdentures supported by either 2 standard Straumann dental implants or 4 Mini Dental Implants (MDIs).de edentate mandibula (prothese met weinig retentie)edentulous mandible (lower jaw)10019190
NL-OMON38808ACTA DENTAL RESEARCH BV64