Comparative Effectiveness of Cystine Versus Nicotine Replacement Therapy

Sponsor
Loma Linda University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04126135
Collaborator
Pfizer (Industry), Mongolian National University of Medical Sciences (Other)
700
1
2
13.1
53.5

Study Details

Study Description

Brief Summary

A pragmatic, single blinded, randomized, controlled non-inferiority trial of Cytisine versus Nicotine Replacement Therapy for continuous abstinence is conducted in the government run primary health hospitals in Mongolia.

Condition or Disease Intervention/Treatment Phase
Phase 3

Detailed Description

Rationale: In Mongolia, smoking cessation assistance in the governmental health sector consists of behavioral counseling and a 3-week regimen of the NRT patch that costs 175 USD. This cost for low income adults limits effectiveness. A 2014 study documented the superiority and lower cost (<20 USD) of Cytisine versus NRT for continuous abstinence. Trial investigators are testing the comparative effectiveness of Cytisine in the "real life setting" of their national health care system and, if proven effective, will include coverage for Cytisine in the national health plan.

Research Question/Objective: To determine whether a 25 day course of Cytisine tablets is at least as effective as 25 days of NRT in helping smokers remain abstinent for at least one month.

Design: A pragmatic, single blinded, randomized, controlled non-inferiority trial.

Setting: Nine governmental primary care centers in Ulaanbaatar, Mongolia, and outskirts.

Participants: Mongolian adult smokers referred to government-run addiction units.

Intervention and procedures: Participants are randomized to 5 weeks of treatment (n=352) or usual care (n=352) and a 6-month follow-up. The treatment consists of a 25-day course of Cytisine tablets and behavioral counseling. Usual care consists of 25 days of NRT and behavioral counseling.

Measurements: The primary outcome is continuous abstinence (< 5 cigarettes smoked since quit date) at 1 month. Secondary outcomes include 7-day point prevalence abstinence rates and adverse events.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
700 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Comparative Effectiveness of Cystine Versus Nicotine Replacement Therapy (NRT) in the National Smoking Cessation Program of Mongolia: A Pragmatic Non-Inferiority Trial
Actual Study Start Date :
Jan 27, 2022
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Usual Care Group

Subjects are asked to completely stop smoking on their quit day and use a daily Nicotine Replacement Therapy (NRT) patch for 25 days.

Drug: Nicotine Replacement Therapy (NRT)
Subjects are asked to completely stop smoking on their quit day and use a daily NRT patch for 25 days.

Experimental: Treatment Group

Subjects will start a 25-day course of Cytisine tablets started during the four days before the quit date and are asked to reduce smoking during this time.

Drug: Cytisine
Subjects will take a 25-day course of Cytisine tablets started during the 4 days before the quit date. They will be asked to reduce smoking during this time.

Outcome Measures

Primary Outcome Measures

  1. Length of abstinence after 25 day course of Cytisine. [One month after quit date]

    Continuous abstinence is defined as <5 cigarettes smoked since quit date. Subjects will complete survey to determine number of cigarettes smoked since quit day.

Secondary Outcome Measures

  1. Length of abstinence after 25 days of NRT [One month after quit date]

    Continuous abstinence is defined as <5 cigarettes smoked since quit date. Subjects will complete survey to determine number of cigarettes smoked since quit day.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Seeking smoking cessation treatment

  • Ages 18 years or older

  • Currently smoking > 5 cigarettes per day

  • Willingness to make quit attempt with pharmacotherapy

  • Able to provide verbal and written informed consent

  • Have telephone access

Exclusion Criteria:
  • Pregnancy or currently breastfeeding

  • Current users of NRT (patch, gum, lozenge)

  • Current users of non_NRT smoking cessation pharmacotherapy

  • Enrolled in another smoking cessation program (non-governmental)

  • Clinical disorder that contraindicates use of NRT or Cytisine (heart attack, stroke, severe angina within the past 2 weeks, uncontrolled hypertension, phaeochromocytoma, severe mental illness)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mongolian National University of Medical Sciences Ulaanbaatar Mongolia

Sponsors and Collaborators

  • Loma Linda University
  • Pfizer
  • Mongolian National University of Medical Sciences

Investigators

  • Principal Investigator: Pramil N Singh, DrPH, Loma Linda University Health
  • Principal Investigator: Davaalkham Dambadarjaa, MD, Mongolian National University of Medical Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Loma Linda University
ClinicalTrials.gov Identifier:
NCT04126135
Other Study ID Numbers:
  • 5170400
First Posted:
Oct 15, 2019
Last Update Posted:
Feb 17, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
Yes
Keywords provided by Loma Linda University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 17, 2022