Treatment of Chemotherapy-related Hiccups With Baclofen

Sponsor
Second Affiliated Hospital of Nanchang University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03778281
Collaborator
(none)
120
4
12.3

Study Details

Study Description

Brief Summary

Hiccup is one of the common side effects of chemotherapy. Intractable hiccups seriously affect patients' rest and eating, reduce the quality of life, and increasingly attract the attention of oncologists. At present, drugs or methods for treating chemotherapy-related hiccups are generally ineffective, with short remission time, serious adverse reactions, and unsatisfactory clinical effects. Baclofen produces skeletal muscle relaxation and was originally used in patients with spinal cord injury, and has since been used to treat intractable hiccups caused by diaphragmatic spasm. This study was an open-label, randomized, prospective study comparing the efficacy and adverse effects of baclofen versus metoclopramide in the treatment of chemotherapy-related hiccups. Patients with hiccup after chemotherapy were randomly divided into two groups. One group was treated with baclofen and the other group was treated with metoclopramide. The efficacy and adverse reactions of the two groups were compared.Ineffective in the two groups will cross to another group and then observe the efficacy.

Condition or Disease Intervention/Treatment Phase
Phase 4

Detailed Description

Hiccup is due to paroxysmal paralysis of the diaphragm, sudden inhalation of gas accompanied by rapid glottis closure and a short high-pitched sound, commonly known as "snoring", is one of the common adverse reactions of chemotherapy. Intractable hiccups seriously affect the rest and eating of patients, reduce the quality of life, and increasingly attract the attention of oncologists. At present, the drugs or methods used in the treatment of chemotherapy-related hiccups mainly include chlorpromazine, Ritalin, diazepam, phenacetin, metoclopramide and traditional Chinese medicine, but these drugs or treatments usually have poor efficacy and short remission time. The adverse reactions were serious and the clinical use was not satisfactory. Baclofen is a gamma-aminobutyric acid (GABA) derivative that activates the GABA-β receptor, inhibits the release of excitatory neurotransmitters, and reduces monosynaptic or multisynaptic transmission in the spinal cord. Skeletal muscle relaxation, originally used in patients with spinal cord injury, is gradually used to treat intractable hiccups caused by diaphragmatic spasm.

This study was an open-label, randomized, prospective study comparing the efficacy and adverse effects of baclofen versus metoclopramide in the treatment of chemotherapy-related hiccups. Patients with hiccup after chemotherapy were randomly divided into two groups. One group was treated with baclofen and the other group was treated with metoclopramide. The efficacy and adverse reactions of the two groups were compared.Ineffective in the two groups will cross to another group and then observe the efficacy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Single (Participant)
Masking Description:
Patient privacy needs to be protected
Primary Purpose:
Treatment
Official Title:
Open-label Randomized Controlled Prospective Study of Baclofen in the Treatment of Chemotherapy-related Hiccups
Anticipated Study Start Date :
Dec 12, 2018
Anticipated Primary Completion Date :
Dec 11, 2019
Anticipated Study Completion Date :
Dec 20, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Baclofen group

Treatment of Chemotherapy-related Hiccups With Baclofen

Drug: Baclofen
Oral baclofen 10mg, 3 times a day for three days, then evaluate the efficacy and side effects
Other Names:
  • Baclofenum、Gabalon、Lioresal
  • Other: Methoxyclopramide group

    Treatment of Chemotherapy-related Hiccups With Methoxyclopramide

    Drug: Methoxyclopramide
    Intramuscular injection of metoclopramide 10mg, 3 times a day for three days, then evaluate the efficacy and side effects
    Other Names:
  • Detoxification
  • Experimental: Baclofen group 2

    After 3 days, if the metoclopramide treatment is ineffective, it will cross into the baclofen group 2.

    Drug: Baclofen
    Oral baclofen 10mg, 3 times a day for three days, then evaluate the efficacy and side effects
    Other Names:
  • Baclofenum、Gabalon、Lioresal
  • Other: Methoxyclopramide group 2

    After 3 days, if the baclofen treatment is ineffective, it will cross into the metoclopramide group 2.

    Drug: Methoxyclopramide
    Intramuscular injection of metoclopramide 10mg, 3 times a day for three days, then evaluate the efficacy and side effects
    Other Names:
  • Detoxification
  • Outcome Measures

    Primary Outcome Measures

    1. Effective rate [3 days]

      Effective rate includes complete response rate and partial response rate

    Secondary Outcome Measures

    1. Adverse reactions [3 days]

      Adverse reactions include drowsiness, dizziness, sedation, tremors, etc.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Pathological diagnosis of malignant tumors;PS score 0 ~ 3 points;

    • Hiccups occurred within 48 h after chemotherapy, lasting longer than 2 h.

    Exclusion Criteria:
    • No serious heart, brain, lung, kidney and other diseases, no gastrointestinal bleeding, no serious obstacles to blood clotting;

    • Blood routine and normal electrolyte of liver and kidney function before chemotherapy.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Second Affiliated Hospital of Nanchang University

    Investigators

    • Study Director: long Huang, Phd, Second Affiliated Hospital of Nanchang University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Second Affiliated Hospital of Nanchang University
    ClinicalTrials.gov Identifier:
    NCT03778281
    Other Study ID Numbers:
    • HL002
    First Posted:
    Dec 19, 2018
    Last Update Posted:
    Dec 19, 2018
    Last Verified:
    Dec 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Second Affiliated Hospital of Nanchang University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 19, 2018