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A Pilot Study of Efficacy of Lactobacillus CD2 Lozenges in Preventing High-dose Chemotherapy Induced Oral Mucositis in Patients Undergoing Hematopoietic Stem Cell Transplantation

Primary Purpose

Oral Mucositis

Status
Completed
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
lactobacillus CD2 lozenges
Sponsored by
All India Institute of Medical Sciences, New Delhi
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Oral Mucositis focused on measuring Lactobacillus CD2 lozenges, high-dose chemotherapy induced, hematopoietic stem cell transplantation

Eligibility Criteria

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

Inclusion Criteria:

  1. Age between 10 and 70 years.
  2. Karnofsky Performance Score ≥ 70%.
  3. Confirmed histological diagnosis of cancer/leukaemia for which haematopoietic stem cell transplantation is an approved modality of therapy.
  4. Patients eligible to receive high-dose chemotherapy as part of conditioning regime.
  5. Concomitant co morbid condition if present, controlled by medicines.
  6. Serum creatinine 1.8mg/dl.
  7. Total bilirubin 2mg/dl.
  8. Liver enzymes within three times of normal limit.
  9. Expected survival > 6 months.

Exclusion Criteria:

  1. Pregnant women and lactating mothers.
  2. Patients with history of AIDS
  3. Patients who have taken any other investigational product in last 4 weeks.
  4. Patients having untreated symptomatic dental infection.
  5. Patients with WHO Grade 3 or 4 oral Mucositis.
  6. Other serious concurrent illness.
  7. Inconclusive histological diagnosis.
  8. Patients on anticancer antibiotics.
  9. Patients with signs and symptoms of systemic infections.
  10. Patient's/guardian's refusal to sign informed consent.

Sites / Locations

  • All India institute of Medical sciences

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

lactobacillus lozenges

Arm Description

The study drug contains not less than 2x109 (2 billion) viable cells of Lactobacillus CD2 as active ingredient

Outcomes

Primary Outcome Measures

incidence of grade III and grade IV mucositis
Determine the incidence of grade III and IV mucositis in patients undergoing allogeneic or autologous haematopoietic stem cell transplantation .

Secondary Outcome Measures

grade I and grade II mucositis
Determine the incidence of Grade I and II mucositis in patients undergoing allogenic or autologous haematopoietic stem cell transplantation. Duration of and time period for healing of chemotherapy induced oral mucositis. Determine incidence and severity of dysphagia

Full Information

First Posted
November 4, 2011
Last Updated
February 19, 2013
Sponsor
All India Institute of Medical Sciences, New Delhi
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1. Study Identification

Unique Protocol Identification Number
NCT01480011
Brief Title
A Pilot Study of Efficacy of Lactobacillus CD2 Lozenges in Preventing High-dose Chemotherapy Induced Oral Mucositis in Patients Undergoing Hematopoietic Stem Cell Transplantation
Official Title
A Pilot Study of Efficacy of Lactobacillus CD2 Lozenges in Preventing High-dose Chemotherapy Induced Oral Mucositis in Patients Undergoing Hematopoietic Stem Cell Transplantation
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
All India Institute of Medical Sciences, New Delhi

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with various malignancies who are taken up for high dose chemotherapy followed by stem cell transplant (blood and marrow transplant) have very high chances of developing severe oral mucositis (between 95-100%). This mucositis not only causes significant morbidity but also hampers quality of life so much so that patients at times feel difficult to continue treatment. No definite treatment exists for prevention or treatment of oral mucositis in this group of patients. Though one study has suggested that use of IV palifermin (a keratinocyte growth factor) will reduce duration and severity. Palifermin is very expensive and not available in country. Recently the investigators have shown effectiveness of a probiotic Lactobacillus CD 2 in reducing incidence and severity of chemo-radiotherapy induced mucositis in head and neck squamous cell cancer patients. (Published online in European Journal of Cancer: http://dx.doi.org/10.1016/j.ejca.2011.06.010). No significant toxicity has been reported with its use. Now, the investigators want to study the efficacy of this drug to reduce severity of mucositis in patients undergoing hematopoietic stem cell transplantation. The drug will be supplied by CD Pharma India Private Limited. The investigators further give undertaking that study will be carried as per good clinical practices (GCP) and declaration of Helsinki.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oral Mucositis
Keywords
Lactobacillus CD2 lozenges, high-dose chemotherapy induced, hematopoietic stem cell transplantation

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
31 (Actual)

8. Arms, Groups, and Interventions

Arm Title
lactobacillus lozenges
Arm Type
Experimental
Arm Description
The study drug contains not less than 2x109 (2 billion) viable cells of Lactobacillus CD2 as active ingredient
Intervention Type
Drug
Intervention Name(s)
lactobacillus CD2 lozenges
Other Intervention Name(s)
CD#2
Intervention Description
The study drug contains not less than 2x109 (2 billion) viable cells of Lactobacillus CD2 as active ingredient
Primary Outcome Measure Information:
Title
incidence of grade III and grade IV mucositis
Description
Determine the incidence of grade III and IV mucositis in patients undergoing allogeneic or autologous haematopoietic stem cell transplantation .
Time Frame
Day 24 of stem cell infusion or complete healing of mucositis
Secondary Outcome Measure Information:
Title
grade I and grade II mucositis
Description
Determine the incidence of Grade I and II mucositis in patients undergoing allogenic or autologous haematopoietic stem cell transplantation. Duration of and time period for healing of chemotherapy induced oral mucositis. Determine incidence and severity of dysphagia
Time Frame
Day 24 of stem cell infusion or complete healing of mucositis

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 10 and 70 years. Karnofsky Performance Score ≥ 70%. Confirmed histological diagnosis of cancer/leukaemia for which haematopoietic stem cell transplantation is an approved modality of therapy. Patients eligible to receive high-dose chemotherapy as part of conditioning regime. Concomitant co morbid condition if present, controlled by medicines. Serum creatinine 1.8mg/dl. Total bilirubin 2mg/dl. Liver enzymes within three times of normal limit. Expected survival > 6 months. Exclusion Criteria: Pregnant women and lactating mothers. Patients with history of AIDS Patients who have taken any other investigational product in last 4 weeks. Patients having untreated symptomatic dental infection. Patients with WHO Grade 3 or 4 oral Mucositis. Other serious concurrent illness. Inconclusive histological diagnosis. Patients on anticancer antibiotics. Patients with signs and symptoms of systemic infections. Patient's/guardian's refusal to sign informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Atul Sharma, MD,DM
Organizational Affiliation
Dr BRA Institute Rotary Cancer Hospital ,All India Institute of Medical Sciences,New Delhi ,India.
Official's Role
Principal Investigator
Facility Information:
Facility Name
All India institute of Medical sciences
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110029
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
21741230
Citation
Sharma A, Rath GK, Chaudhary SP, Thakar A, Mohanti BK, Bahadur S. Lactobacillus brevis CD2 lozenges reduce radiation- and chemotherapy-induced mucositis in patients with head and neck cancer: a randomized double-blind placebo-controlled study. Eur J Cancer. 2012 Apr;48(6):875-81. doi: 10.1016/j.ejca.2011.06.010. Epub 2011 Jul 6.
Results Reference
result
PubMed Identifier
28848667
Citation
Sharma A, Tilak T, Bakhshi S, Raina V, Kumar L, Chaudhary S, Sahoo R, Gupta R, Thulkar S. Lactobacillus brevis CD2 lozenges prevent oral mucositis in patients undergoing high dose chemotherapy followed by haematopoietic stem cell transplantation. ESMO Open. 2017 Feb 13;1(6):e000138. doi: 10.1136/esmoopen-2016-000138. eCollection 2016.
Results Reference
derived

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A Pilot Study of Efficacy of Lactobacillus CD2 Lozenges in Preventing High-dose Chemotherapy Induced Oral Mucositis in Patients Undergoing Hematopoietic Stem Cell Transplantation

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