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Use of Intranasal Oxytocin During Detoxification of Crack Cocaine

Primary Purpose

Cocaine Withdrawal, Cocaine Smoking, Cocaine-Related Disorders

Status
Unknown status
Phase
Phase 1
Locations
Brazil
Study Type
Interventional
Intervention
Oxytocin nasal spray
placebo nasal spray
Sponsored by
Pontificia Universidade Católica do Rio Grande do Sul
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cocaine Withdrawal focused on measuring crack cocaine, addiction, stimulants, oxytocin, detoxification, abstinence, withdrawal

Eligibility Criteria

18 Years - 52 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Volunteers (no payment to be enroll in the research according with Brazilian legislation)
  • Age 18-52 years
  • Primary diagnosis of cocaine crack dependence according to DSM-5
  • Sex feminine
  • Participants must be abstinent at least 7 days prior the study intervention
  • Participants must consent to be randomly allocated to experimental conditions

Exclusion Criteria:

  • Pregnancy
  • Puerperium
  • Breastfeeding
  • Menopause
  • Currently using hormone therapy
  • Total hysterectomy
  • Diagnosis or suspicion of autoimmune or neurological diseases and / or syndromes (stroke, Parkinson and Alzheimer's)
  • Diagnosis or suspected current decompensated and / or severe endocrine, cardiovascular, pulmonary, renal, gastrointestinal disorders
  • Moderate or severe psychotic syndrome
  • Obesity Level III
  • Intellectual impairment (IQ <70)
  • Corticosteroid therapy, glucocorticoid or any exogenous steroid therapy
  • Infectious condition or acute febrile syndrome
  • Significant nasal congestion
  • Type III nasal septum deviation (cases considered severe with deviated septum in which breathing is impaired)
  • Mucosal lesions
  • History of head trauma moderate or severe (Glasgow <12)
  • HIV +

Sites / Locations

  • Hospital Santa AnaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Placebo Comparator

No Intervention

Arm Label

Conventional oxytocin treatment (T + OC)

Conventional treatment with placebo administration (T + PBO)

Conventional treatment (T)

Arm Description

32 female cocaine users hospitalized for detoxification will receive six 4 IU jets of intranasal oxytocin twice daily (daily dose of 48 IU) as adjunctive treatment to conventional treatment from the eighth to seventeenth day of hospitalization (duration of oxytocin treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization.

32 female cocaine users hospitalized for detoxification will receive six jets of placebo solution (2% odor-generating propolis essence + the same vehicle as intra-nasal oxytocin: 0.05% citric acid, 0.9% sodium chloride, 1% glycerol, 0.54% disodium phosphate, 0.2% methylparaben + propylparaben, 1% sorbitol, 80% water) twice daily as adjunctive treatment to conventional treatment from the eighth to the seventeenth day of hospitalization (duration of placebo treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization.

32 female cocaine users hospitalized for detoxification will receive conventional treatment including individual and group supportive psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy if needed for symptom relief. anxiety, aggression and agitation, typical of abstinence and nursing care, during 21 days of hospitalization.

Outcomes

Primary Outcome Measures

Withdrawal symptoms
Change from baseline withdrawal symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by Cocaine Selective Severity Assessment (CSSA, minimum and maximum scores: 0 - 112). After treatment, the oxytocin-treated group is expected to have significantly lower withdrawal scores (better outcome) than the other groups (30%).
Anxiety symptoms
Change from baseline anxiety symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by the Patient-Reported Outcomes Measurement Information System Short Form scale (PROMIS, minimum and maximum raw scores: 8 - 40). After treatment, the oxytocin-treated group is expected to show lower anxiety scores (better outcome) compared to the other groups (30%).
Depression symptoms
Change from baseline depressive symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by the Quick Inventory of Depressive Symptomatology Self-Report scale (QIDS-SR, minimum and maximum scores: 0 - 27). After treatment, the oxytocin-treated group is expected to show lower depressive scores (better outcome) compared to the other groups (30%).

Secondary Outcome Measures

Neuroleptic Dose Change
Dose change of neuroleptic medications used during hospitalization for agitation or irritability (expected 25% lower).
Adherence of outpatient treatment
Rate of adherence of outpatient treatment six months after discharge (expected to be 20% higher) assessed by reviewing the medical records of each patient within the outpatient program. If patient would be enrolled in the outpatient program after six months from detoxification she will be considered adhered to the program (higher rates means better outcome).

Full Information

First Posted
March 9, 2020
Last Updated
March 11, 2020
Sponsor
Pontificia Universidade Católica do Rio Grande do Sul
Collaborators
Secretaria Nacional de Políticas sobre Drogas (SENAD), Conselho Nacional de Desenvolvimento Científico e Tecnológico
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1. Study Identification

Unique Protocol Identification Number
NCT04306354
Brief Title
Use of Intranasal Oxytocin During Detoxification of Crack Cocaine
Official Title
Randomized, Double-Blind, Placebo Controlled Study of Intranasal Oxytocin During Detoxification of Crack Cocaine
Study Type
Interventional

2. Study Status

Record Verification Date
March 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 15, 2018 (Actual)
Primary Completion Date
April 30, 2020 (Anticipated)
Study Completion Date
May 31, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Pontificia Universidade Católica do Rio Grande do Sul
Collaborators
Secretaria Nacional de Políticas sobre Drogas (SENAD), Conselho Nacional de Desenvolvimento Científico e Tecnológico

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Randomized treatment control trial, double-blind, parallel, with two arms including ninety-six hospitalized women between 18 and 52 years. Those who agree to participate in the study and meet the eligibility criteria will be randomly allocated to one of the following experimental conditions: Conventional oxytocin treatment (T + OC): 32 female cocaine users hospitalized for detoxification will receive six 4 IU jets of intranasal oxytocin twice daily (daily dose of 48 IU) as adjunctive treatment to conventional treatment from the eighth to seventeenth day of hospitalization (duration of oxytocin treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization. Conventional treatment with placebo administration (T + PBO): 32 female cocaine users hospitalized for detoxification will receive six jets of placebo solution (2% odor-generating propolis essence + the same vehicle as intra-nasal oxytocin: 0.05% citric acid, 0.9% sodium chloride, 1% glycerol, 0.54% disodium phosphate, 0.2% methylparaben + propylparaben, 1% sorbitol, 80% water) twice daily as adjunctive treatment to conventional treatment from the eighth to the seventeenth day of hospitalization (duration of placebo treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization. Conventional treatment (T): 32 female cocaine users hospitalized for detoxification will receive conventional treatment including individual and group supportive psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy if needed for symptom relief. anxiety, aggression and agitation, typical of abstinence and nursing care, during 21 days of hospitalization. Outcomes: Withdrawal symptoms, Anxiety symptoms and Depressive symptoms
Detailed Description
Design: Randomized treatment control trial, double-blind, parallel, with two arms. Sample: Ninety-six hospitalized women between 18 and 52 years will participate in this study. Those who agree to participate in the study and meet the eligibility criteria will be randomly allocated to one of the following experimental conditions: Conventional oxytocin treatment (T + OC): 32 female cocaine users hospitalized for detoxification will receive six 4 IU jets of intranasal oxytocin twice daily (daily dose of 48 IU) as adjunctive treatment to conventional treatment from the eighth to seventeenth day of hospitalization (duration of oxytocin treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization. Conventional treatment with placebo administration (T + PBO): 32 female cocaine users hospitalized for detoxification will receive six jets of placebo solution (2% odor-generating propolis essence + the same vehicle as intra-nasal oxytocin: 0.05% citric acid, 0.9% sodium chloride, 1% glycerol, 0.54% disodium phosphate, 0.2% methylparaben + propylparaben, 1% sorbitol, 80% water) twice daily as adjunctive treatment to conventional treatment from the eighth to the seventeenth day of hospitalization (duration of placebo treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization. Conventional treatment (T): 32 female cocaine users hospitalized for detoxification will receive conventional treatment including individual and group supportive psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy if needed for symptom relief. anxiety, aggression and agitation, typical of abstinence and nursing care, during 21 days of hospitalization. Inclusion Criteria: Volunteers (no payment to be enroll in the research according with Brazilian legislation) Age 18-52 years Primary diagnosis of cocaine crack dependence according to DSM-5 Sex feminine Participants must be abstinent at least 7 days prior the study intervention Participants must consent to be randomly allocated to experimental conditions Exclusion Criteria: Pregnancy Puerperium Breastfeeding Menopause Currently using hormone therapy Total hysterectomy Diagnosis or suspicion of autoimmune or neurological diseases and / or syndromes (stroke, Parkinson and Alzheimer's) Diagnosis or suspected current decompensated and / or severe endocrine, cardiovascular, pulmonary, renal, gastrointestinal disorders Moderate or severe psychotic syndrome Obesity Level III Intellectual impairment (IQ <70) Corticosteroid therapy, glucocorticoid or any exogenous steroid therapy Infectious condition or acute febrile syndrome Significant nasal congestion Type III nasal septum deviation (cases considered severe with deviated septum in which breathing is impaired) Mucosal lesions History of head trauma moderate or severe (Glasgow <12) HIV + Primary Outcome Measure: Withdrawal symptoms Change from baseline withdrawal symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by Cocaine Selective Severity Assessment (CSSA, minimum and maximum scores: 0 - 112). After treatment, the oxytocin-treated group is expected to have significantly lower withdrawal scores (better outcome) than the other groups (30%). Anxiety symptoms Change from baseline anxiety symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by the Patient-Reported Outcomes Measurement Information System Short Form scale (PROMIS, minimum and maximum raw scores: 8 - 40). After treatment, the oxytocin-treated group is expected to show lower anxiety scores (better outcome) compared to the other groups (30%). Depression symptoms Change from baseline depressive symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by the Quick Inventory of Depressive Symptomatology Self-Report scale (QIDS-SR, minimum and maximum scores: 0 - 27). After treatment, the oxytocin-treated group is expected to show lower depressive scores (better outcome) compared to the other groups (30%). Secondary Outcome Measures: Neuroleptic Dose Change Dose change of neuroleptic medications used during hospitalization for agitation or irritability (expected 25% lower). Adherence of outpatient treatment Rate of adherence of outpatient treatment six months after discharge (expected to be 20% higher) assessed by reviewing the medical records of each patient within the outpatient program. If patient would be enrolled in the outpatient program after six months from detoxification she will be considered adhered to the program (higher rates means better outcome).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine Withdrawal, Cocaine Smoking, Cocaine-Related Disorders
Keywords
crack cocaine, addiction, stimulants, oxytocin, detoxification, abstinence, withdrawal

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
On the eve of the eighth day of hospitalization, a person in charge of the research team performed a randomization of the participants exchanged in blocks, according to the methods of Schulz and collaborators (SCHULZ; GRIMES, 2002). The responsible person did not have contact with the participants. The blocks were made up of 12 participants each, and the ratio was maintained at 4: 4: 4, in order to reduce the chances of the groups getting mixed amounts. The members of the research team responsible for data collection, the technical team of the inpatient unit and the participants did not know to what condition each patient had been allocated. These procedures guaranteed the randomization and double blinding of the study.
Allocation
Randomized
Enrollment
96 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional oxytocin treatment (T + OC)
Arm Type
Experimental
Arm Description
32 female cocaine users hospitalized for detoxification will receive six 4 IU jets of intranasal oxytocin twice daily (daily dose of 48 IU) as adjunctive treatment to conventional treatment from the eighth to seventeenth day of hospitalization (duration of oxytocin treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization.
Arm Title
Conventional treatment with placebo administration (T + PBO)
Arm Type
Placebo Comparator
Arm Description
32 female cocaine users hospitalized for detoxification will receive six jets of placebo solution (2% odor-generating propolis essence + the same vehicle as intra-nasal oxytocin: 0.05% citric acid, 0.9% sodium chloride, 1% glycerol, 0.54% disodium phosphate, 0.2% methylparaben + propylparaben, 1% sorbitol, 80% water) twice daily as adjunctive treatment to conventional treatment from the eighth to the seventeenth day of hospitalization (duration of placebo treatment of 10 days). Conventional treatment includes supportive individual and group psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy as needed to relieve the symptoms of anxiety, aggression and agitation typical of withdrawal and care. 21 days of hospitalization.
Arm Title
Conventional treatment (T)
Arm Type
No Intervention
Arm Description
32 female cocaine users hospitalized for detoxification will receive conventional treatment including individual and group supportive psychotherapy (once a week), nutritional control, regular physical activity and psychopharmacotherapy if needed for symptom relief. anxiety, aggression and agitation, typical of abstinence and nursing care, during 21 days of hospitalization.
Intervention Type
Drug
Intervention Name(s)
Oxytocin nasal spray
Intervention Description
Oxytocin nasal spray 24 UI twice daily as adjunctive treatment to conventional treatment during 10 days of detoxification of crack cocaine
Intervention Type
Drug
Intervention Name(s)
placebo nasal spray
Intervention Description
Nasal spray with placebo solution (2% odor-generating propolis essence + the same vehicle as intra-nasal oxytocin: 0.05% citric acid, 0.9% sodium chloride, 1% glycerol, 0.54% disodium phosphate, 0.2% methylparaben + propylparaben, 1% sorbitol, 80% water) twice daily as adjunctive treatment to conventional treatment.
Primary Outcome Measure Information:
Title
Withdrawal symptoms
Description
Change from baseline withdrawal symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by Cocaine Selective Severity Assessment (CSSA, minimum and maximum scores: 0 - 112). After treatment, the oxytocin-treated group is expected to have significantly lower withdrawal scores (better outcome) than the other groups (30%).
Time Frame
Change from baseline (first week after hospital admission) at the end of detoxification treatment (21 days).
Title
Anxiety symptoms
Description
Change from baseline anxiety symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by the Patient-Reported Outcomes Measurement Information System Short Form scale (PROMIS, minimum and maximum raw scores: 8 - 40). After treatment, the oxytocin-treated group is expected to show lower anxiety scores (better outcome) compared to the other groups (30%).
Time Frame
Change from baseline (first week after hospital admission) at the end of detoxification treatment (21 days).
Title
Depression symptoms
Description
Change from baseline depressive symptoms (hospital admission) at the end of detoxification treatment (21 days) assessed by the Quick Inventory of Depressive Symptomatology Self-Report scale (QIDS-SR, minimum and maximum scores: 0 - 27). After treatment, the oxytocin-treated group is expected to show lower depressive scores (better outcome) compared to the other groups (30%).
Time Frame
Change from baseline (first week after hospital admission) at the end of detoxification treatment (21 days).
Secondary Outcome Measure Information:
Title
Neuroleptic Dose Change
Description
Dose change of neuroleptic medications used during hospitalization for agitation or irritability (expected 25% lower).
Time Frame
Change from baseline (first week after hospital admission) at the end of detoxification treatment (21 days)
Title
Adherence of outpatient treatment
Description
Rate of adherence of outpatient treatment six months after discharge (expected to be 20% higher) assessed by reviewing the medical records of each patient within the outpatient program. If patient would be enrolled in the outpatient program after six months from detoxification she will be considered adhered to the program (higher rates means better outcome).
Time Frame
six months after hospital discharge

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
52 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Volunteers (no payment to be enroll in the research according with Brazilian legislation) Age 18-52 years Primary diagnosis of cocaine crack dependence according to DSM-5 Sex feminine Participants must be abstinent at least 7 days prior the study intervention Participants must consent to be randomly allocated to experimental conditions Exclusion Criteria: Pregnancy Puerperium Breastfeeding Menopause Currently using hormone therapy Total hysterectomy Diagnosis or suspicion of autoimmune or neurological diseases and / or syndromes (stroke, Parkinson and Alzheimer's) Diagnosis or suspected current decompensated and / or severe endocrine, cardiovascular, pulmonary, renal, gastrointestinal disorders Moderate or severe psychotic syndrome Obesity Level III Intellectual impairment (IQ <70) Corticosteroid therapy, glucocorticoid or any exogenous steroid therapy Infectious condition or acute febrile syndrome Significant nasal congestion Type III nasal septum deviation (cases considered severe with deviated septum in which breathing is impaired) Mucosal lesions History of head trauma moderate or severe (Glasgow <12) HIV +
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rodrigo Grassi-Oliveira, MD, PhD
Phone
+555133203633
Email
rodrigo.grassi@pucrs.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodrigo Grassi-Oliveira, MD, PhD
Organizational Affiliation
Pontifícia Universidade Católica do Rio Grande do Sul
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Santa Ana
City
Porto Alegre
State/Province
RS
ZIP/Postal Code
91720-440
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
João Vitor Nobrega, MD
First Name & Middle Initial & Last Name & Degree
Rodrigo Grassi-Oliveira, MD, PhD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
By the time of publication
IPD Sharing Access Criteria
open access

Learn more about this trial

Use of Intranasal Oxytocin During Detoxification of Crack Cocaine

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