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Intravenous Haloperidol as an adjuvant analgesic for management of cancer pai

Phase 2
Conditions
Health Condition 1: - Health Condition 2: C00-D49- Neoplasms
Registration Number
CTRI/2023/10/058922
Lead Sponsor
Cancer Institute WIA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)All patients who are diagnosed with abdominal cancer and, head and neck cancer, receiving morphine for pain management, in acute severe pain NRS = 7

2)Age 18 – 65 years

Exclusion Criteria

1)People who are already on psychiatric medications or previous psychiatric disorder

2)People in acute delirium or mentally incapacitated or has severe emotional or psychiatric disorder.

3)People with history or current evidence of QT prolongation arrythmia or existing cardiovascular problems

4)People with extrapyramidal symptoms or existing parkinsonism

5)People who are hypotensive, hypothyroid, increased liver function tests

6)People who are allergic to haloperidol

7)People not consenting for the study or inability to give informed consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the effect of intravenous haloperidol as an adjuvant analgesic in treating acute cancer pain among patients visiting the Palliative care Outpatient Department.Timepoint: numerical rating scale will be assessed for pain at 0 minutes, 15 minutes, 30 minutes, 45 minutes and at the end of 1 hour
Secondary Outcome Measures
NameTimeMethod
1.To assess the patient reported onset and duration of response to intravenous haloperidol. <br/ ><br>2.To determine the dose of haloperidol to attain adequate analgesia. <br/ ><br>3.To observe the side effects of administration of intravenous haloperidol <br/ ><br>4.To assess the feasibility of performing the study in the palliative care outpatient department <br/ ><br>Timepoint: within 2 days of intervention
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