AzTrials
AzTrials

Dermatitis, Radiation InducedANTAGELNCT07207889

Retrospective Analysis of the Efficacy of Morphine Gel to Treat Pain Associated With Perineal RadioDermatitis

An observational study of Dermatitis, Radiation Induced, run by Institut Curie at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Retrospective study evaluating the efficacy of a pharmacy-prepared Morphine gel used in clinics for the treatment of pain associated with perineal radiodermatitis. The main aim of this study is to evaluate the efficacy of Morphine Gel (MG) in pain management. Read more about this study

Who is it for?
Ages 18 to 100 years
Conditions the study is for
Dermatitis, Radiation Induced
What is being tested?
morphine chlorhydrate in intrasite gel
How many people
17 participants
Where
1 siteFrance
Study dates
1 Dec 2024to 31 Dec 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 100 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: 17 patients who received Morphine gel for the treatment of pain associated with perineal radiodermatitis over a 20-month period between July 2022 and March 2024.

Who may be able to join

  • Patients 18 years and older;
  • Use of a local analgesic treatment based on Morphine gel for pain associated with perineal radiodermatitis.
  • Patients not relieved by prescribed systemic treatments (per-os or intravenous)
  • Patients treated with radiotherapy for a perineal tumor, whether or not associated with medical treatment such as chemotherapy.
  • Minimum grade of radiodermatitis: Grade II

Who cannot join

  • Patients who have not used the prescribed morphine gel
  • Minor patients
  • Patients using morphine gel for wounds other than radiodermatitis
  • Patients who object to the re-use of their data

Trial locations and contacts

1 site in 1 country.

France1 site
  • Institut Curie

    Paris, 75248

Other trials in France

About this study

Official title: Retrospective Analysis of the Efficacy of Morphine Gel (MG) for the Treatment of Pain Associated With RadioDermatitis (RD) More Than Grade II

Retrospective study evaluating the efficacy of a pharmacy-prepared Morphine gel used in clinics for the treatment of pain associated with perineal radiodermatitis. The main aim of this study is to evaluate the efficacy of Morphine Gel (MG) in pain management.

Read the detailed description

Radiotherapy (RT) can induce acute side effects or toxicities, known as radiodermatitis (RD). Technological and technical advances have made it possible to reduce these toxicities (1), although certain organs such as the skin and mucous membranes remain vulnerable, particularly when the tumor is located nearby.

Skin exposed to ionizing radiation (IR) during the treatment of tumors close to the cutaneous surface is no longer able to renew itself due to an alteration in the basal cell mitotic process, leading to suppression of skin cell renewal. IR also induces senescence of epidermal keratinocytes, responsible for exacerbated inflammatory activity and structural dysfunction of the epidermal barrier, through disruption of the keratinization and cornification process. (2).

RD usually heals ad integrum. They are classified into 5 grades according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0 (3), presenting different clinical aspects ranging from grade I to V.

Grade II and III RDs are frequently observed in patients undergoing perineal RT, especially as medical treatment is associated.

In addition to the tumor's proximity to the skin, several anatomical factors specific to the perineal region contribute to the occurrence of these RDs: a wetter area, with skin folds, subject to friction and the presence of the urinary and anal orifices, potential sources of irritation by the elimination of urine and feces.

These RD are painful and have a significant impact on patients' quality of life (4,5,6). Pain intensity is often underestimated prior to treatment (7). The discomfort and pain experienced during RT intensify over the course of the sessions (8). Although RD is a frequent acute toxicity in patients treated for perineal tumors, there are few studies describing the impact of RD-related pain. The treatment of pain in RT must be rigorously assessed, and appropriate systemic or local therapy proposed (9). The challenge in treating pain in perineal radiodermatitis (PDR) is to ensure the full administration of the initial RT treatment regimen, which in the event of long interruption or premature discontinuation would expose the patient to a greater risk of recurrence (10-12).

Despite the studies carried out, there is no consensus on local care for the prevention or treatment of DR. However, the topicals used should not compromise the efficacy of RT, and should optimize healing, with gels being the preferred form.

This is why a dedicated care circuit has been set up at the Institut Curie to optimize preventive skin care and monitoring of tolerance to ROP. This system enables the early detection of painful ROP refractory to the prescribed systemic treatment.

In case of painful RD: patients are offered a hydrogel preparation mixed with morphine for local relief. Patients apply this preparation themselves during the day.

The main objective of this study is to evaluate the efficacy of morphine gel (GM) in the treatment of pain in PRD. The primary endpoint is the patient's self-reported reduction in pain. Secondary objectives include evaluation of systemic analgesic prescription and analysis of treatment interruptions attributable to DR.

Being tested
morphine chlorhydrate in intrasite gel
Keywords
morphine gel, cutaneous toxicity
Medical subject headings
Radiodermatitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • morphine chlorhydrate in intrasite gelDrug

    The use of Morphine gel to treat painfull perineal radiodermatitis is new. None clinical study was conducted to explore the efficacy of the morphine gel as local analgesic for these cutaneous toxicity due to radiotherapy

Study groups in NCT07207889
Study groupRoleWhat they receive
Patients using morphine gelpatients who received morphine gel to treat pain due to perineal radiodermatitis
Receives: Drug: morphine chlorhydrate in intrasite gel

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Efficacy of morphine gel (GM) in the treatment of pain in perineal radiodermatitis

    Reduced pain as assessed by the patient. Verbal scale to qualify the evolution of the pain (decreased - stable - increased)

    Measured: between baseline and day2 to day21

Secondary outcomes (2)
  1. Assessment of systemic analgesic prescribed

    Difference of type of non-opoïd and opioïd treatment prescribed from baseline to D2 to D21.

    Measured: between baseline and day2 to day 21

  2. Interruption of radiotherapy treatment in connection with radiodermatitis

    Number of radiotherapy treatment breaks or discontinuation

    Measured: during 5 weeks from first day of radiotherapy (throught radiotherapy completion)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2025
  2. Study start1 Dec 2024
  3. Primary completion31 Dec 2024
  4. Study completion31 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
17 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07207889
Sponsor's protocol ID
DATA240316 ANTAGEL
Acronym
ANTAGEL
Status last verified
Apr 2025
First submitted
29 Aug 2025
Last updated
6 Oct 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Dermatitis, Radiation Induced, run by Institut Curie at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Efficacy of morphine gel (GM) in the treatment of pain in perineal radiodermatitis (time frame: between baseline and day2 to day21). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in