Intravenous vs Oral Analgesia in Cancer Patients With Severe Pain After Successful Titration

Sponsor

Fujian Cancer Hospital (Other)

Overall Status

Completed

CT.gov ID

NCT04243954

Collaborator

(none)

Enrollment

Location

Arms

7.4

Actual Duration (Months)

12.9

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Pain is one of the most common and fear symptoms for cancer patients, which seriously affects the quality of life in cancer patients. At present, oral opioid is the most common route to administrate cancer pain. However, the patients do not satisfy the pain administration with oral opioid after successful titration in many cases, especially the cases with severe cancer pain. Patient controlled analgesia (PCA) with hydromorphone can take analgesic effect rapidly. The aim of this trial is to compare the maintenance with hydromorphone PCA intravenously or switch to Sustained-Release Morphine orally after successful titraton with hydromorphone PCA intravenously in severe cancer pain.

Condition or Disease	Intervention/Treatment	Phase
Cancer Pain	Drug: PCA IV Hydromorphone (continuous dose = 0) Drug: PCA IV Hydromorphone (continuous dose ≠ 0) Drug: Oral morphine	Phase 2

Study Design

Study Type:

Interventional

Actual Enrollment :

95 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Hydromorphone PCA Intravenously vs Sustained-Release Morphine Orally in Cancer Patients With Severe Pain After Successful Titration: A Multicenter, Randomized, Controlled, Phase II Trial

Actual Study Start Date :

Apr 10, 2020

Actual Primary Completion Date :

Oct 21, 2020

Actual Study Completion Date :

Nov 21, 2020

Arms and Interventions

Arm	Intervention/Treatment
Experimental: PCA IV Hydromorphone (continuous dose = 0) Intravenous PCA with hydromorphone after successful titration of 24 hours. The PCA setting: 1) Continuous dose = 0; 2) Bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours: 3) Lockout time = 10 minutes; 4) Evaluate once every 24 hours	Drug: PCA IV Hydromorphone (continuous dose = 0) Intravenous PCA with hydromorphone after successful titration of 24 hours. the PCA setting: 1) continuous dose = 0; 2) bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours: 3) lockout time = 10 minutes; 4) evaluate once every 24 hours
Experimental: PCA IV Hydromorphone (continuous dose ≠ 0) Intravenous PCA with hydromorphone after successful titration of 24 hours. The PCA setting: 1) Continuous dose (dose/hours) = the total dosage of hydromorphone in the previous 24 hours/24; 2) Bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours; 3) Lockout time = 10 minutes; 4) Evaluate once every 24 hours	Drug: PCA IV Hydromorphone (continuous dose ≠ 0) Intravenous PCA with hydromorphone after successful titration of 24 hours. the PCA setting: 1) continuous dose (dose/hours) = the total dosage of hydromorphone in the previous 24 hours/24; 2) bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours; 3) lockout time = 10 minutes; 4) evaluate once every 24 hours
Active Comparator: Oral Morphine Swift to sustained-release morphine orally as background dose with immediate release morphine orally for breakthrough pain after successful titration of 24 hours. Administration of morphine orally 1) Sustained-release morphine orally (dose/12 hours) = the total equianalgesic of the previous 24 hours/2×75% for d1; the total equianalgesic of the previous 24 hours/2 for day 2 and day 3; 2) Immediate release morphine orally = 10-20% of the total equianalgesic of the previous 24 hours; 3) Evaluate once every 24 hours	Drug: Oral morphine Swift to sustained-release morphine orally as background dose with immediate release morphine orally for breakthrough pain after successful titration of 24 hours. Administration of morphine orally 1) Sustained-release morphine orally (dose/12 hours) = the total equianalgesic of the previous 24 hours/2×75% for d1; the total equianalgesic of the previous 24 hours/2 for day 2 and day 3; 2) Immediate release morphine orally = 10-20% of the total equianalgesic of the previous 24 hours; 3) Evaluate once every 24 hours

Arm

Intervention/Treatment

Experimental: PCA IV Hydromorphone (continuous dose = 0)

Intravenous PCA with hydromorphone after successful titration of 24 hours. The PCA setting: 1) Continuous dose = 0; 2) Bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours: 3) Lockout time = 10 minutes; 4) Evaluate once every 24 hours

Drug: PCA IV Hydromorphone (continuous dose = 0)

Intravenous PCA with hydromorphone after successful titration of 24 hours. the PCA setting: 1) continuous dose = 0; 2) bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours: 3) lockout time = 10 minutes; 4) evaluate once every 24 hours

Experimental: PCA IV Hydromorphone (continuous dose ≠ 0)

Intravenous PCA with hydromorphone after successful titration of 24 hours. The PCA setting: 1) Continuous dose (dose/hours) = the total dosage of hydromorphone in the previous 24 hours/24; 2) Bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours; 3) Lockout time = 10 minutes; 4) Evaluate once every 24 hours

Drug: PCA IV Hydromorphone (continuous dose ≠ 0)

Intravenous PCA with hydromorphone after successful titration of 24 hours. the PCA setting: 1) continuous dose (dose/hours) = the total dosage of hydromorphone in the previous 24 hours/24; 2) bolus dose = 10-20% of the total dosage of hydromorphone in the previous 24 hours; 3) lockout time = 10 minutes; 4) evaluate once every 24 hours

Active Comparator: Oral Morphine

Swift to sustained-release morphine orally as background dose with immediate release morphine orally for breakthrough pain after successful titration of 24 hours. Administration of morphine orally 1) Sustained-release morphine orally (dose/12 hours) = the total equianalgesic of the previous 24 hours/2×75% for d1; the total equianalgesic of the previous 24 hours/2 for day 2 and day 3; 2) Immediate release morphine orally = 10-20% of the total equianalgesic of the previous 24 hours; 3) Evaluate once every 24 hours

Drug: Oral morphine

Outcome Measures

Primary Outcome Measures

Mean pain score [From day1 to day3]
The Numerical Rating Scale (NRS, a score of 0 means no pain and 10 means the most severe) is used to assess the severity of pain. NRS of 24 hours is assessed every day. The mean pain score is a sum of NRS of day 1 (the day after successful titration of 24 hours) to day 3 divided by 3. If the NRS of the morphine orally group >3, the NRS in the hydromorphone PCA intravenously group declines more than 30% compared to morphine orally group, which is regards a positive result.
Number of Breakthrough cancer Pain (BTcP) episodes [From day1 to day3]
If NRS of the morphine orally group pain score ≤3 , or if NRS in the hydromorphone PCA intravenously group declines less than 30% compared to morphine orally group, number of Breakthrough cancer Pain (BTcP) episodes in the one of both the hydromorphone PCA intravenously group declines less than 30% compared to morphine orally group, which is regards a positive result.

Secondary Outcome Measures

Number of patients with an average NRS pain score> 3 [From day1 to day3]
The Numerical Rating Scale (NRS, a score of 0 means no pain and 10 means the most severe) is used to assess the severity of pain.
Number of patients with an average NRS pain score> 6 [From day1 to day3]
The Numerical Rating Scale (NRS, a score of 0 means no pain and 10 means the most severe) is used to assess the severity of pain.
Total dosage of opioids [3 days]
The total dosage of opioids in day 1 to day 3 (day 1 is the day after successful titration of 24 hours)
Satisfaction score [3 days]
The satisfaction score of the patients to analgesia was evaluated by 10-point scale: 0 points for dissatisfaction, 10 points for very satisfied, the higher the score, the higher the satisfaction.
Quality of life of patients [At 24 hours]
Chinese version of the Edmonton Symptom Assessment System.
Number of patients who switched/discontinued therapy due to serious adverse events or lack of pain control [3 days]
The number of patients who switched/discontinued therapy due to serious adverse events or lack of pain control

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 80 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

The patients were 18-80 years old and diagnosed as malignant tumor by pathology;
Patients with cancer pain is NRS pain score ≥ 7 during previous 24 hours;
Patients who will not be treated with radiotherapy within 7 days prior to randomization and during study ;
Patients who need chemotherapy, long term administration of hormone, targeted therapy, or bisphosphonates therapy should undergo a stable anti- tumor therapy prior to randomization ;
Patients or his/her caregivers who are able to fill out the questionnaire forms ;
Ability to correctly understand and cooperate with medication guidance of doctors and nurses ;
Without psychiatric problems;
ECOG performance status ≤3;
Not participated in another drug clinical trial within one month before inclusion（including hydromorphone）;
The subjects voluntarily signed the informed consent.

Exclusion Criteria:

The pain is confirmed not due to cancer;
Patients with severe post-operative pain;
Patients with paralytic ileus;
Patients with brain metastasis;
Patients hypersensitive to opioids;
Patients with abnormal lab results that have obvious clinical significance, such as creatine ≥ 2 fold of upper limit of normal value, alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≥ 2.5 fold of upper limit of normal value, or liver function of Child C grade;
Patients who cannot take drugs orally;
Patients with an incoercible nausea or vomiting;
Those who have received monoamine oxidase inhibitor (MAOI) within two weeks before randomization;
Patients who are pregnant or in lactation, or who plan to be pregnant within one month after the trial;
Those with opioid addiction;
Alcoholic patients;
Those with cognitive dysfunction;
Those with severe depression;
Patients with other conditions or reasons causing the patients unable to complete the clinical trial.