Clinical Trial: EValuation of the Impact of a TOpical Lotion on Permanent Chemotherapy Induced Hair Disorders in Cancer Survivors
Study Status: Active, not recruiting
Recruit Status: Active, not recruiting
Study Type: Interventional
Official Title: EValuation of the Impact of a TOpical Lotion, CG428, on Permanent Chemotherapy Induced Hair and Scalp Disorders in Cancer SUrvivors: A randoMized, Single-center, Double-blind placEbo Controlled Trial
Brief Summary:
This study aims to evaluate the Impact of a topical Lotion, CG428, on permanent chemotherapy induced hair and scalp disorders in Cancer survivors. This is a double-blind, single center, randomized, controlled trial in breast cancer survivors.
Hair condition and parameters of 61 breast cancer survivors who were previously included in DERMA study (a prospective cohort study to assess appearance changes due to breast cancer treatment completed in July, 13th,2013) will be assessed.
- Patients whose hair parameters are below the baseline as measured before the start of the chemotherapy or
- who complain from incomplete hair regrowth will be eligible to participate in the randomized controlled trial.
Patients who agree to participant in the study will be randomly assigned to two parallel arms (Arm 1: CG428/ Arm 2: Placebo). Patients will self-administer the study product or placebo twice per day (morning, evening) for 6 months, for the efficacy assessment.
Primary endpoint was recovery of hair thickness 6 months after intervention as assessed using Folliscope 4.0.
Secondary endpoints included hair density at 6 months after intervention, distress due to chemotherapy induced alopecia, scalp skin parameters (water and sebum). Patient-reported hair quality improvement, body image and quality of life, and time to first visible improvement based on global photographs of hair and nails.
Detailed Summary: The research team at Cancer Education Center at Samsung Comprehensive Cancer Center has studied CIA and its impact on distress and psychosocial well-being since 2008. We found that more than half of the breast cancer patients experienced higher distress due to CIA, during cancer treatment, and this distress was strongly associated with negative body image, overall health status, and psychosocial well-being. In a recent prospective cohort study, we assessed skin and hair change patterns before, during and 6 months after chemotherapy in 61 volunteers. We found that the majority of the patients still experienced CIA at 6 months after completion of chemotherapy. Actually, hair diameter at 6th month after chemotherapy had not recovered to baseline level. Permanent chemotherapy-induced alopecia, defined as absent or incomplete hair regrowth at ≥6 months post-chemotherapy, was reported from 53 to 74%. Like CIA, permanent CIA also lacks recognition and has been underserved regardless of patients' needs. The first botanical blend Legacy Healthcare developed and patented is Cellium. Cellium is composed of 4 botanicals (Allium cepa L., Citrus limon L., Theobroma cacao L., Paullinia cupana). The first product derived from Cellium is a topical lotion for male and female alopecia, CG210. Based on the safety and efficacy data, the EMA (European Medicines Agency) has considered CG210 eligible for a European centralized herbal medicine registration. CG428 is the second product derived from Cellium. CG428 contains the exact same ingredients as CG210, in a different dosage. Legacy Healthcare have conducted a pilot studies with CG428 in Japan. The trial included female cancer survivors experiencing permanent/persistent CIA for more than 12. Based on the results, several cancer treatment centers in Japan have started to recommend the product on a compassionate basis.We therefore hypothesize that the investigated topical lotion may mitigate the impact of protracted or permanent CIA
Sponsor: Samsung Medical Center
Current Primary Outcome: Recovery rate of hair thickness 6 months after intervention Using Folliscope 4.0, LeadM [ Time Frame: 6 months after randomization ]
Original Primary Outcome: Same as current
Current Secondary Outcome:
- Chemotherapy-induced alopecia distress Stress Using Chemotherapy induced alopecia distress scale (CADS) [ Time Frame: 6 months after randomization ]Respondents will be instructed to indicate on a 4-point Likert scale on each statement (1=Not at all, 2= A little, 3=Quite a bit, 4=Very much). Total scores will be calculated by summing responses for all items; higher scores means more distress due to CIA
- Global photographs [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]Pictures to be focused on head/hair, which means shorter distance between the equipment and the subject using Canon EOS 70D
- Scalp skin water levels [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]Water on scalp: it will be measured using Corneometer (Courage-Khazakaelectronic GmbH, Germany). We will measure 3 times on same area
- Sebum on scalp [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]it will be measured using Sebumeter SM815 (Courage-Khazakaelectronic GmbH, Germany). We will measure 1 times on same area
- Overall hair and scalp condition [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]Patient self-assessment: We will measure patient reported hair density and thickness, scalp condition, and density using visual analogue scale (VAS) ranging from 0 to 10
- Nail condition [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]
Patient self-assessment: We will use self-reported questionnaire using visual analogue scale (VAS) ranging from 0 to 10.
Global photographs: We will take a picture the patients' nail using Canon EOS 70D with Intelli-Flash system or similar system
- Quality of life [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]We will assess patients' body image using European Organization for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaire Core 30 and breast specific module
- Depression [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]We will assess patients' depression using Hospital Anxiety and Depression Scale (HADS). It consists of 14 items in two domains (Depression and anxiety).
- Anxiety [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]We will assess patients' anxiety using Hospital Anxiety and Depression Scale (HADS). It consists of 14 items in two domains (Depression and anxiety).
- Satisfaction with products [ Time Frame: After intervention (3month and 6 months after intervention) ]We will use self-reported questionnaire for satisfaction with the products as well as suggestions for improvement after completion of study with patients who received the CG428.
- Hair condition [ Time Frame: All time (baseline, 3month and 6 months after intervention) ]
Outcomes will be collected using objective methods and patient reported outcomes:
Objectively quantified: Hair thickness and density: We will measure hair thickness and density using Folliscope 4.0, LeadM We will take a picture on the parietal (To around 2 cm) and then analysis using Folliscope program.
Global photographs: Pictures to be focused on head/hair, which means shorter distance between the equipment and the subject
Original Secondary Outcome: Chemotherapy-induced alopecia distress Stress Using Chemotherapy induced alopecia distress scale (CADS) [ Time Frame: 6 months after randomization ]
Information By: Samsung Medical Center
Dates:
Date Received: November 10, 2015
Date Started: January 2016
Date Completion: August 2017
Last Updated: December 6, 2016
Last Verified: December 2016
