Not provided
Not provided
Not provided
Not provided
Recruiting patients too low
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Assistance Publique - Hôpitaux de Paris | OTHER |
| Hôpital Louis Mourier | OTHER |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
This phase III study aims to show that topical morphine low doses treats localized pain in chronic wounds, intense and rebellious to systemic analgesics included or not opioids.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Morphine gel | Experimental | morphine 30 mg, quantity of gel per application: 15mg (15ml) |
|
| Neutral gel | Placebo Comparator | water for injection, quantity of gel per application: 15mg (15ml) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Morphine gel | Drug | Topical |
| |
| Neutral gel |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of patients whose maximum daily consumption in immediate-release oral morphine is less than or equal to 30 mg for the last 72 hours of the study | Proportion of patients whose maximum daily consumption in immediate-release oral morphine is less than or equal to 30 mg (either up to 3 tablets 10 mg per day) for the last 72 hours of the study (day 8 to day 11) and for which the basic treatment is unchanged throughout the duration of the study | 11 days |
| Measure | Description | Time Frame |
|---|---|---|
| Reduction in average daily pain intensity score on a numerical rating scale self assessment, measured on an 11-point between day 1 and day 11 | Reduction in average daily pain intensity score on a numerical rating scale (where 0=no pain and 10=worst possible pain) self assessment, measured on an 11-point between day 1 and day 11. Therefore patients evaluate each morning local pain of the previous 24 hours. |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Valerie LAURENT, MD | Institut Curie - Hôpital René Huguenin | Principal Investigator |
| Audrey Hurgon, MD | Institut Curie Paris | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpital Louis Mourier | Colombes | Île-de-France Region | 92700 | France | ||
| Institut Curie |
Not provided
Not provided
Not provided
Not provided
Not provided
| Other |
Topical |
|
| 11 days |
| Evaluate the percentage of local pain relief for 24 hours on a rating scale from 0 to 100% | 11 days |
| Assess and characterize the evolution of local pain on a global impression scale change : Pain related Patient Global Impression of Change (PGIC) and Clinical Global Impression of Change (CGIC) | 11 days |
| Assess patient satisfaction with treatment of local pain (score 0-4) | 11 days |
| Evaluate the impact score of local pain on sleep (self-report scale of 0 to 100%) | 0% no impact of pain on sleep 100% maximum impact of pain on sleep, inability to sleep | 11 days |
| Determine the time (in hours) before using oral immediate-release morphine after application of local treatment | 11 days |
| Determination of cumulative dose of oral immediate-release morphine (in milligrams) of the 11 days of treatment for relieving painful access of local origin | 11 days |
| Evaluate systemic and local side effects of analgesic treatment (incidence, severity and location) | 11 days |
| Evaluate the systemic absorption of topical morphine blood test after the first application | 11 days |
| Paris |
| Île-de-France Region |
| 75005 |
| France |
| Hôpital Jean-Jaurès | Paris | Île-de-France Region | 75019 | France |
| Groupe Hospitalier Bichat | Paris | Île-de-France Region | 75877 | France |
| Institut Curie - Hôpital René Huguenin | Saint-Cloud | Île-de-France Region | 92210 | France |