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Rectal CancerPhase 3RECTILNCT06123156

Interest of Early Erectile Rehabilitation With Sildenafil After Radiotherapy and Proctectomy for Rectal Cancer

A Phase 3 study testing Sildenafil in people with Rectal Cancer, run by University Hospital, Rouen at 14 sites in France.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study aims to evaluate the efficacy of erectile rehabilitation with Sildenafil, in men treated with neoadjuvant proctectomy and radiotherapy for rectal cancer, in preventing long-term erectile dysfunction at 12 months post-operatively. Read more about this study

Who is it for?
Ages 18 to 70 years, men only
Conditions the study is for
Rectal Cancer
What is being tested?
Sildenafil
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
188 participants
Where
14 sitesFrance
Study dates
25 Sep 2025to Feb 2030
Phase
Phase 3
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 to 70 years
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Men aged 18 to 70
  • Patients undergoing surgery for cancer of the lower or middle rectum by total removal of the mesorectum with colorectal or coloanal anastomosis after neoadjuvant radiotherapy, with normal preoperative erectile function (defined by a combined IIEF erectile function domain score of at least 22).
  • Nerve-conserving surgery
  • Sexually active patient without treatment for erectile function prior to surgery
  • Presence of a regular sexual partner (male or female)
  • Adult having read and understood the information letter and signed the consent form
  • Membership of a social security scheme

Who cannot join

  • T4 tumor or tumor requiring extended surgery
  • Patients with abnormal erectile function defined by a combined IIEF erectile function domain score of less than 22.
  • History of prostate cancer
  • Sleep disorders, patients taking sedatives/hypnotics
  • Contraindication to SILDENAFIL EG 50 mg, film-coated tablet
  • Contraindication to placebo
Show all 11Show fewer
  • Patients already treated with PDE5 inhibitors
  • Patients suffering from SARS COV 2*
  • Person deprived of liberty by an administrative or judicial decision or person placed under court protection / sub-guardianship or guardianship.
  • Any history of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for participation in the protocol, or to prevent the subject from giving informed consent.
  • Person participating in another drug trial.

Trial locations and contacts

14 sites in 1 country. Contact the study team or a site near you to ask about taking part.

14 sites in 1 country

France14 sites, 14 recruiting
  • Chu Amiens

    Amiens, 80054

    Charles Sabbagh, Pr, 03 22 08 88 93, Sabbagh.charles@chu-amiens.fr

    Charles Sabbagh, Pr

    Recruiting
  • Hopital Beauvais

    Beauvais, 60000

    François Mauvais, Pr, 03 44 11 26 26, f.mauvais@ch-beauvais.fr

    François Mauvais, Pr

    Recruiting
  • Chu Besancon

    Besançon, 25030

    Zaher Lakkis, Dr, 03 81 66 93 44, zlakkis@chu-besancon.fr

    Zaher Lakkis, Dr

    Recruiting
  • Aphp Bicetre

    Bicêtre, 94275

    Stéphane Benoist, Pr, 01 45 21 70 30, stephane.benoist@aphp.fr

    Stéphane Benoist, Pr

    Recruiting
  • Chu Bordeaux

    Bordeaux, 33000

    Benjamin Fernandez, Dr, 05 56 79 58 10, benjamin.fernandez@chu-bordeaux.fr

    Benjamin Fernandez, Dr

    Recruiting
  • Institut Bordeaux Colorectal

    Bordeaux, 33000

    Quentin Denoist, Dr, 05 47 50 15 75, q.denost@bordeaux-colorectal-institute.fr

    Quentin Denoist, Dr

    Recruiting
  • Chu Clermont-Ferrand

    Clermont-Ferrand, 63000

    Anne Dubois, Dr, 04 73 75 05 32, a_dubois@chu-clermontferrand.fr

    Anne Dubois, Dr

    Recruiting
  • Chu Lille

    Lille, 59000

    Guillaume Piessen, Dr, 03 20 44 44 07, guillaume.piessen@chru-lille.fr

    Guillaume Piessen, Dr

    Recruiting
  • Institut Paoli-Calmettes

    Marseille, 13009

    Marie Dazza, Dr, 06 83 32 41 77, dazzam@ipc.unicancer.fr

    Marie Dazza, Dr

    Recruiting
  • Institut Du Cancer Montpellier

    Montpellier, 34000

    Philippe Rouanet, Pr, 04 67 61 30 71, Philippe.Rouanet@icm.unicancer.fr

    Philippe Rouanet, Pr

    Recruiting
  • Aphp St Antoine

    Paris, 75012

    Jérémie Lefevre, Dr, 01 49 28 26 87, jeremie.lefevre@aphp.fr

    Jérémie Lefevre, Dr

    Recruiting
  • Aphp Hegp

    Paris, 75908

    Medhi Karoui, Pr, 01 56 09 35 34, mehdi.karoui@aphp.fr

    Medhi Karoui, Pr

    Recruiting
  • Chu Rouen

    Rouen, 76031

    Julien Coget, Dr, 02 32 88 82 83, julien.coget@chu-rouen.fr

    Julien Coget, Dr

    Recruiting
  • Chu Tours

    Tours, 37000

    Mehdi Ouaissi, Pr, 02 18 37 05 75, m.ouaissi@chu-tours.fr

    Mehdi Ouaissi, Pr

    Recruiting

Other trials in France

About this study

Official title: Intérêt de la rééducation érectile précoce Par Sildénafil après radiothérapie et Proctectomie Pour Cancer du Rectum : Essai contrôlé randomisé

This study aims to evaluate the efficacy of erectile rehabilitation with Sildenafil, in men treated with neoadjuvant proctectomy and radiotherapy for rectal cancer, in preventing long-term erectile dysfunction at 12 months post-operatively.

Read the detailed description

Colorectal cancer is the third most common cancer in men in France, after lung and prostate cancer. Proctectomy (possibly preceded by radiotherapy) is the most effective treatment for this cancer, but erectile dysfunction (ED) is a frequent complication, even when the nerves are preserved during dissection, and has a major impact on the quality of life of operated men.

The cause of erectile dysfunction after rectal cancer surgery is usually neurological, due to intraoperative trauma to the autonomic nerves, while erectile dysfunction after radiotherapy is mainly vascular in origin, with damage to erectile tissue.

Several risk factors for sexual dysfunction after rectal cancer surgery have been reported (age, neoadjuvant radiotherapy, type of resection, operative difficulties and complications, body image affected by protective stoma). On the other hand, surgical expertise may be a protective factor.

In the physiological condition, the nitric oxide released by the pelvic nerves causes an increase in cyclic guanosine monophosphate, which in turn causes smooth muscle cells relaxation and an influx of blood into the cavernous body, triggering and maintaining the erection.

Similar to prostatectomy, nerve damage can occur during proctectomy through stretching, heat, ischemia or inflammation; this nerve damage results in reduced nitric oxide production.

Even in the absence of nerve damage, it has been demonstrated (in an animal model) that post-operative neurapraxia is responsible for the at least temporary disappearance of spontaneous and nocturnal erections, leading to cavernous hypoxia. This is followed by tissue changes (reduction in smooth and elastic muscle fibers in the corpora cavernosa, increase in collagen and endothelial dysfunction), which modify the hemodynamics of the carvernum body and ultimately lead to fibrosis of the erectile tissue.

These changes can become permanent despite subsequent nerve recovery, and are exacerbated by neoadjuvant radiotherapy. It is therefore important not to wait passively for erectile function to be restored, as lack of oxygenation to the corpora cavernosa can lead to permanent fibrosis and dysfunction.

This physiopathology is at the origin of the concept of erectile rehabilitation after prostatectomy, with the aim of maintain erections post-operatively and thus limiting fibrosis.

The benefits of erectile re-education after prostatectomy were first reported in 1997, with the early use of intracavernous injections of alprostadil. Following this study, various rehabilitation strategies have been recommended. Early treatment, i.e. within the first month, is recommended to promote cavernous oxygenation and prevent fibrosis.

The aims of rehabilitation are as follows :

  • limit fibrosis;
  • limit penis retraction and loss of height;
  • oxygenate the cavernum body;
  • preserve endothelial structure;
  • preserve smooth muscle cell structure.

Various types of rehabilitation have been proposed: oral PDE-5 inhibitors, intra-cavernosal injections, urethral suppositories or vaccum.

PDE-5 inhibitors prevent the degradation of cyclic guanosine monophosphate, thus compensating for the reduction in nitric oxide and enabling a better erection.

Erectile rehabilitation using PDE-5 inhibitors could protect cavernous smooth muscle from irreversible pathophysiological changes. The basic concept is to administer a PDE-5 inhibitor at bedtime to facilitate nocturnal erections, which are thought to have a natural protective effect on the function of the cavernous bodies.

Padma-Nathan et al. reported the prospective administration of sildenafil 50 and 100 mg vs. placebo, daily and at bedtime, in patients undergoing nerve-sparing radical prostatectomy. After 36 weeks, erectile function was significantly better in the sildenafil group, with 27% responders, vs. 4% in the placebo group.

The mechanisms involved in erectile dysfunction after proctectomy for rectal cancer are similar to those of radical prostatectomy for prostate cancer.

The efficacy of PDE-5 inhibitors in the treatment of erectile dysfunction after proctectomy has already been demonstrated. However, its use as a preventive measure has rarely been reported.

Three studies have evaluated PDE-5 inhibitors in patients with erectile dysfunction after rectal resection, two of which used sildenafil (Viagra, Pfizer, New York, NY)

To our knowledge, only one study has evaluated the role of PDE-5 inhibitors (PDE-5i) in a preventive strategy.

Originality and innovation Despite the fact that sexual dysfunction is recognized as a frequent complication of rectal cancer treatment, there are currently no recommendations for its prevention and management.

In contrast to prostate cancer patients, information and treatment concerning erectile dysfunction (ED) are not systematically offered to men with colorectal cancer. The ability of sildenafil to facilitate the return of erections after radical prostatectomy has been demonstrated in several studies, and this treatment could benefit patients treated for rectal cancer.

To date, no randomized study has examined the usefulness of this early rehabilitation in patients managed for rectal cancer. This study proposes, for the first time, to evaluate the use of sildenafil after neo-adjuvant radiotherapy and surgery for rectal cancer.

Conditions
Rectal Cancer
Being tested
Sildenafil, Placebo
Medical subject headings
Rectal Neoplasms

What participants receive

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

  • SildenafilDrug

    Also called Arm I

    Sildénafil during 10 months (50mg daily), start 30 days after surgery

  • PlaceboOther

    Also called Arm II

    1 platelet during 10 months (daily), start 30 days after surgery

Study groups in NCT06123156
Study groupRoleWhat they receive
Arm I (Sildénafil)Active comparatorSildénafil during 10 months (50mg daily), start 30 days after surgery
Receives: Drug: Sildenafil
Arm II (Placebo)Placebo comparatorPatients receive placebo during 10 month (1 platelet per day)
Receives: Other: Placebo

What is being measured

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

  1. the patient's response

    A patient is defined as a responder by a score of at least 22 for the erectile function domain of the International Index of Erectile Function (IIEF), comprising the six IIEF questions relating to erection (Q1-Q5 and Q15).

    Measured: 12 months postoperatively

Secondary outcomes (9)
  1. IIEF erectile function domain score

    Mesure of IIEF erectile function domain score, comprising the six IIEF erectile function questions (Q1-Q5 andQ15) at D0, M1, M3, M6, M9 and M12

    Measured: Day 0, Month 1, Month 3, Month 6, Month 9, Month12

  2. International Index of Erectile Function (IIEF) global score

    International Index of Erectile Function (IIEF) global score measured at D0, M1, M3, M6, M9 and M12

    Measured: Day 0, Month 1, Month 3, Month 6, Month 9, Month 12

  3. Quality of life score

    Mesure of quality of life score (EORTC QLQ - C30 and QLQ - CR29) at D0, M1, M3, M6, M9 and M12

    Measured: Day 0, Month 1, Month 3, Month 6, Month 9, Month 12

  4. LARS score

    LARS score measured at D0, M1, M3, M6, M9 and M12

    Measured: Day 0, Month 1, Month 3, Month 6, Month 9, Month 12

  5. Fecal Continence Score

    Fecal Continence Score (Wexner score) measured at D0, M1, M3, M6, M9 and M12

    Measured: Day 0, Month 1, Month 3, Month 6, Month 9, Month 12

  6. Spontaneous erection evaluation

    Number of patients with spontaneous erections on treatment at M3, M6, M9 and without treatment at M1, and M12

    Measured: Month 1, Month 3, Month 6, Month 9, Month 12

  7. Benefits of psychological follow-up

    The number of patients with or without regular psychological follow-up. A patient is defined as having regular follow-up if he/she visits a psychologist and/or psychiatrist once or twice a month.

    Measured: after 10 months of treatment

  8. Compliance with treatment

    Number of unused tablets during the study. The patient will be considered as non-compliant if pill-taking over the entire 10-month treatment period is <80%.

    Measured: after 10 months of treatment

  9. Adverse and suspected adverse events

    Number of AEs and SAEs in each group at M1, M3, M6, M9 and M12

    Measured: Month 1, Month 3, Month 6, Month 9, Month 12

Timeline

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

  1. First posted8 Nov 2023
  2. Study start25 Sep 2025
  3. Primary completionFeb 2030 (estimated)
  4. Study completionFeb 2030 (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 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
188 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06123156
Sponsor's protocol ID
2019/0398/HP
Other IDs
2020-002682-34
Acronym
RECTIL
Status last verified
May 2026
First submitted
26 Oct 2023
Last updated
12 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Sildenafil in people with Rectal Cancer, run by University Hospital, Rouen at 14 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 7 inclusion and 11 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: looking for participants now, as of the sponsor's last update on 12 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 14 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

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?

Contact Valérie Bridoux (0232881347 ext. +33, valerie.bridoux@chu-rouen.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

the patient's response (time frame: 12 months postoperatively). 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 12 May 2026.

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