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EndometriosisLYVENDONCT07175857

Evaluation of the Efficacy of an Innovative Digital Therapeutic Medical Device, Lyv Endo, for the Management of Patients With Endometriosis

A study testing Lyv Endo app in people with Endometriosis, run by Lyv Healthcare at 8 sites in France.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The main objective of this clinical study is to evaluate the clinical impact of using an innovative digital therapeutic device on the quality of life of patients with endometriosis. Read more about this study

Who is it for?
Ages 18 years and older, women only
Conditions the study is for
Endometriosis
What is being tested?
Lyv Endo app
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
400 participants
Where
8 sitesFrance
Study dates
21 Jul 2025to 30 Sep 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Women ≥18 years old
  • with confirmed endometriosis diagnosis
  • symptomatic patients (NRS ≥ 4 on one or more symptoms)
  • French-speaking
  • Owning a smartphone with internet/data,
  • covered by French social security

Who cannot join

  • Planned surgery during the study or surgery in the past 8 weeks
  • Fertility hormone treatment during study
  • Previous use of full Lyv Endo app or pilot program
  • Pregnant or breastfeeding
  • Under legal protection (guardianship, etc.)
  • Cognitive or psychiatric conditions compromising consent
  • Judged non-autonomous by investigator
  • Participation in another interventional study

Trial locations and contacts

8 sites in 1 country.

8 sites in 1 country

France8 sites
  • Hôpital Privé de Provence

    Aix-en-Provence, France, 13080

  • Clinique Tivoli Ducos

    Bordeaux, 33000

  • CHU CAEN

    Caen, France, 14000

  • Centre Hospitalier de Versailles

    Le Chesnay, 78157

  • Centre Hospitalier Le Mans

    Le Mans, 72000

  • Hôpital Le Blois

    Lille, 59000

  • Hôpital Paris Saint-Joseph

    Paris, 75014

  • CHU Rennes

    Rennes, France, 35000

Other trials in France

About this study

The main objective of this clinical study is to evaluate the clinical impact of using an innovative digital therapeutic device on the quality of life of patients with endometriosis.

The working hypothesis is that the therapeutic digital medical device Lyv Endo may improve quality of life and reduce symptom intensity by enhancing patient engagement in the management of their condition. This justifies the need to evaluate the effect of Lyv Endo as a complement to standard medical care.

Read the detailed description

Endometriosis is a chronic, systemic, and inflammatory disease. Long considered a gynecological condition, endometriosis is now recognized as a systemic disease associated with symptoms and comorbidities that extend well beyond the reproductive system, affecting psychological well-being, social life, and professional activity. Endometriosis affects nearly 10% of women of reproductive age, corresponding to an estimated 1.5 to 2.5 million women in France. It is most commonly diagnosed in women aged 25 to 49 years, who represent 68.3% of cases, whereas women under 25 are rarely diagnosed (fewer than 4%). According to the French Haute Autorité de Santé (HAS), the prevalence of endometriosis may affect between 600,000 and 700,000 women aged 18 to 50 years in France.

Endometriosis is characterized by the presence of endometrium-like tissue outside the uterus, which may lead to severe pain, particularly during menstruation, as well as infertility in approximately one-third of cases. On average, diagnosis is delayed by seven years, complicating the management of the disease. Common symptoms include severe menstrual pain (dysmenorrhea), chronic pelvic pain, deep dyspareunia, dyschezia during menstruation, cyclic urinary symptoms, and infertility.

Diagnosis is primarily clinical, supported by imaging examinations such as transvaginal ultrasound and pelvic MRI to confirm the presence of lesions. In the absence of conclusive findings, empirical treatment may be initiated based on symptom relief, with a presumptive diagnosis. Laparoscopy, previously a routine diagnostic procedure, is now reserved for complex cases where imaging is inconclusive and treatments have failed.

To date, there is no curative treatment for endometriosis. Current treatments are symptomatic and include hormonal therapies (progestins or combined oral contraceptives), hormonal intrauterine devices, and analgesics (e.g., tramadol, nefopam, paracetamol-codeine or paracetamol-tramadol combinations). Up to 83% of patients continue to experience persistent symptoms despite medical or surgical treatment. In cases of severe pain or infertility resistant to treatment, surgical intervention may be considered, although recurrence is possible.

Given the chronic nature of the symptoms, endometriosis is a complex, multifactorial disease requiring multidisciplinary care. An integrative approach-including therapeutic education, regular physical activity, psychological support, and dietary measures-is essential to improve symptom management and patient quality of life. Supportive therapies such as physiotherapy and sophrology have shown benefits in endometriosis patients. These non-pharmacological therapies are increasingly recommended by pain specialists to address central sensitization and help raise pain thresholds, which are pathologically low in patients with chronic pelvic pain. This multimodal and multidisciplinary approach, as a complement to conventional pharmacological treatment, aligns with the HAS recommendations for managing chronic pain, which apply to endometriosis patients.

However, most patients still lack access to such multidisciplinary care. This gap may be partly due to insufficient training in endometriosis among frontline healthcare professionals (e.g., general practitioners and community gynecologists), who are often unaware of the proven benefits of this type of approach and do not refer patients to relevant professionals (e.g., physiotherapists, psychologists, sex therapists). Additionally, the number of healthcare professionals specialized in endometriosis remains limited, especially in medically underserved areas. Finally, due to limited consultation time, healthcare providers may not be able to address all these aspects during routine visits.

Over the past decade, the development of digital technologies and connected devices has opened new perspectives in patient care. These tools can play a crucial role by offering innovative solutions to relieve pain, enhance patient education, and foster greater autonomy in symptom self-management. In the field of endometriosis, there are currently very few digital medical devices specifically dedicated to supporting patients.

The Lyv Endo device is a CE-marked Class I digital therapeutic medical device that stands out through its integrative, patient-centered approach to endometriosis management. Its innovation lies in its ability to deliver comprehensive and personalized content tailored to each patient's symptoms, addressing key limitations of traditional care (e.g., limited consultation time, low availability of trained professionals). This digital medical device offers individualized therapeutic support across five key modules: disease knowledge, mental well-being, adapted physical activity, nutrition, and sexual health. Lyv Endo is positioned at the forefront of digital medical technologies, with the goal of transforming endometriosis care.

The main objective is to evaluate the clinical impact of using an innovative digital therapeutic device on the quality of life of patients with endometriosis.

Secondary Objectives :

  • To evaluate the clinical impact of using the Lyv Endo digital therapeutic on the quality of life of patients with endometriosis
  • To evaluate the clinical impact on symptoms and complications associated with endometriosis
  • To evaluate the clinical impact on mental health
  • To assess the impact on lifestyle habits
  • To assess the organizational impact
  • To assess the health economic impact
  • To evaluate the usability of the full version of the therapeutic digital medical device
Conditions
Endometriosis
Being tested
Lyv Endo app
Keywords
Endometriosis
Medical subject headings
Endometriosis

What participants receive

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

  • Lyv Endo appDevice

    Lyv Endo is a CE-marked Class I therapeutic digital medical device offering a patient-centered, integrative approach. Its innovation lies in its ability to deliver personalized content based on symptoms, surpassing the limits of traditional care.

Study groups in NCT07175857
Study groupRoleWhat they receive
ControlNo interventionstandard care
InterventionExperimentalUse of the Lyv Endo app + standard care
Receives: Device: Lyv Endo app

What is being measured

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

  1. Clinical impact

    Change in Endometriosis Health Profile-5 score ranging from 0 (best outcome) to 100 (worst outcome)

    Measured: Baseline and 3 months

Secondary outcomes (20)
  1. Clinical Impact

    Change in Quality of Life : variation in EuroQol 5-Dimension (EQ-5D-5L) ranging from level 1(no problem) to level 5 (unable to/extreme problems)

    Measured: Baseline and 3 months

  2. Clinical Impact

    Change in Quality of Life: proportion of patients with deterioration of quality of life based on Endometriosis Health Profile-5 (EHP-5) total score (MCID = 4.5 points)

    Measured: 3 months

  3. Clinical Impact

    Change in global symptom intensity: variation in total and subgroup Numeric Rating Scale scores (0 = best outcome; 10 = worst outcome)

    Measured: Baseline and 3 months

  4. Clinical Impact

    Change in Sensitization: variation in Central sensitization inventory (CSI) ranging from 0 (best outcome) to 36 (worst outcome)

    Measured: Baseline and 3 months

  5. Clinical Impact

    Change in depression level: variation in Patient Health Questionnaire-9 (PHQ-9) scores (0 = best outcome; 27 = worst outcome)

    Measured: Baseline and 3 months

  6. Clinical Impact

    Change in anxiety level: variation in Generalized Anxiety Disorder-7 (GAD-7) scores (0 = best outcome; 21 = worst outcome)

    Measured: Baseline and 3 months

  7. Clinical Impact

    Change in associated analgesic consumption: monthly evolution of analgesic use

    Measured: From baseline to 3 months

  8. Clinical Impact

    Change in lifestyle habits: frequency of physical activity

    Measured: Baseline and 3 months

  9. Clinical Impact

    Change in lifestyle habits: percentage of patients with adapted eating behaviors

    Measured: Baseline and 3 months

  10. Clinical Impact

    Change in lifestyle habits: sleep quality

    Measured: Baseline and 3 months

  11. Organisational Impact

    Change in organisational parameters: number of endometriosis-related healthcare visits

    Measured: Baseline and 3 months

  12. Organisational Impact

    Change in organisational parameters: duration of sick leaves

    Measured: Baseline and 3 months

  13. Organisational Impact

    Change in organisational parameters: variation in Work Productivity and Activity Impairment questionnaire (WPAI) scores (0 = best outcome; 10 = worst outcome)

    Measured: Baseline and 3 months

  14. Health Economic impact

    Comparative analysis of health economic parameters: cost-utility analysis

    Measured: 3 months

  15. Health Economic impact

    Description: Comparative analysis of health economic parameters: estimated costs for the French National Health Insurance

    Measured: 3 months

  16. Health Economic Impact

    Comparative analysis of health economic parameters: healthcare resource utilization

    Measured: 3 months

  17. Usability of Therapeutic Digital Medical Device

    Adherence rate

    Measured: From Baseline to 3 months

  18. Usability of Therapeutic Digital Medical Device

    Number of logins

    Measured: From Baseline to 3 months

  19. Usability of Therapeutic Digital Medical Device

    Engagement with the personalized program

    Measured: From Baseline to 3 months

  20. Usability of Therapeutic Digital Medical Device

    Satisfaction level and System Usability Scale (SUS) score (0 = worst outcome; 100 = best outcome)

    Measured: 3 months

Timeline

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

  1. First posted16 Sep 2025
  2. Study start21 Jul 2025
  3. Primary completion30 Sep 2026 (estimated)
  4. Study completion30 Sep 2026 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
400 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07175857
Sponsor's protocol ID
LYVENDO
Acronym
LYVENDO
Status last verified
Jun 2026
First submitted
7 Aug 2025
Last updated
8 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Breton Z, Stern E, Pinault M, Lhuillery D, Petit E, Panel P, Alexaline M. A Digital Program for Daily Life Management With Endometriosis: Pilot Cohort Study on Symptoms and Quality of Life Among Participants. JMIR Form Res. 2025 Feb 28;9:e58262. doi: 10.2196/58262.

    PubMed 39791286
  • Aubry G, Panel P, Thiollier G, Huchon C, Fauconnier A. Measuring health-related quality of life in women with endometriosis: comparing the clinimetric properties of the Endometriosis Health Profile-5 (EHP-5) and the EuroQol-5D (EQ-5D). Hum Reprod. 2017 Jun 1;32(6):1258-1269. doi: 10.1093/humrep/dex057.

    PubMed 28383700
  • O'Hara R, Rowe H, Fisher J. Managing endometriosis: a cross-sectional survey of women in Australia. J Psychosom Obstet Gynaecol. 2022 Sep;43(3):265-272. doi: 10.1080/0167482X.2020.1825374. Epub 2020 Oct 13.

    PubMed 33050751
  • Coxon L, Vollert J, Perro D, Lunde CE, Ferreira-Gomes J, Charrua A, Abreu-Mendes P, Krassowski M, Birch J, Meijlink J, Hummelshoj L, Hoffmann A, Aziz Q, Arendt-Nielsen L, Pogatzki-Zahn E, Evans E, Demetriou L, McMahon SB, Missmer SA, Becker CM, Zondervan KT, Horne AW, Cruz F, Sieberg CB, Treede RD, Nagel J, Vincent K. Comprehensive quantitative sensory testing shows altered sensory function in women with chronic pelvic pain: results from the Translational Research in Pelvic Pain (TRiPP) Study. Pain. 2023 Nov 1;164(11):2528-2539. doi: 10.1097/j.pain.0000000000002955. Epub 2023 Jun 7.

    PubMed 37289573
  • Cohen SP, Vase L, Hooten WM. Chronic pain: an update on burden, best practices, and new advances. Lancet. 2021 May 29;397(10289):2082-2097. doi: 10.1016/S0140-6736(21)00393-7.

    PubMed 34062143
  • Zondervan KT, Becker CM, Missmer SA. Endometriosis. N Engl J Med. 2020 Mar 26;382(13):1244-1256. doi: 10.1056/NEJMra1810764. No abstract available.

    PubMed 32212520

Questions about this trial

What is this clinical trial studying?

A study testing Lyv Endo app in people with Endometriosis, run by Lyv Healthcare at 8 sites 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 6 inclusion and 8 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: under way, not looking for participants, as of the sponsor's last update on 8 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 8 sites 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?

This study is still under way. Results are not available in the source record yet.

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?

Clinical impact (time frame: Baseline and 3 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07175857, which also lists 6 linked publications.

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 8 Jun 2026.

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