CHAMGAP
APPROVEDReviewed and approved by the Chamgap Editorial Team (2026-08-15). The draft was written by AI, the existence of all 3 cited sources was verified at the original page, and the verdict passed blind grading and adversarial audit. Methodology v0.7.
Verdict No. 2680 · Search date 2026-08-15 · Methodology v0.7

Once-daily tadalafil,
does it really help with Increased recovery of unassisted erectile function after treatment cessation?

30-Second Summary
D
Evidence Grade D · 28 · Safety caution
Tadalafil helped erectile function during treatment but did not increase natural recovery after the drug was stopped
Headache, flushing, dyspepsia, back pain, and hypotension can occur. Nitrates are contraindicated because of severe hypotension risk, and post-surgical use requires urologic supervision.
What the
research shows
The grade is D with 28 points. In the 422-person treated REACTT analysis, IIEF-EF at least 22 after nine months of treatment and a six-week drug-free washout occurred in 20.9% with once-daily tadalafil and 19.1% with placebo, OR 1.1 (95% CI 0.6 to 2.1, P=0.675). Erectile function improved while taking the drug, but the prespecified primary claim of unassisted recovery after stopping was null.
What the
ads claim
An erection benefit while taking tadalafil and natural recovery after stopping are different questions. An on-drug secondary result should not be marketed as proof that nerves were rehabilitated.
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Useful facts when choosing a product

  • REACTT used nine months of blinded treatment, six weeks fully off drug, then a three-month open extension.
  • All three selected papers report the same NCT01026818 trial.
  • The registry sponsor and reported funder were Eli Lilly and Company.
Gap Measurement · Verdict 2680 · D 28
What advertising claims
What independent, higher-quality research supports
△ GAP
01

What the research actually shows

Four hundred twenty-three participants were assigned to once daily, 139, on demand, 143, or placebo, 141. One on-demand participant never received study drug, leaving 422 analyzed. After washout, IIEF-EF at least 22 occurred in 20.9%, 16.9%, and 19.1%, respectively. Odds ratios versus placebo were 1.1 (0.6 to 2.1) for daily and 0.9 (0.5 to 1.7) for on demand. The three reports divided main, time-to-recovery, and quality-of-life or satisfaction outcomes from the same REACTT trial; all use NCT01026818 and are not three replications. Eli Lilly funded the trial and employees were coauthors. Randomization, double masking, and double dummy were reported, but the public material reviewed did not establish the implementation method for allocation concealment, so the trial was not treated as defect-free.

02

Why this is classified as D (28)

The primary unassisted-recovery outcome was null, multiple papers were only reports of one manufacturer trial, and the confidence interval left substantial benefit possible, giving D with 28 points.

Counterpoint. Concomitant nitrates can cause dangerous hypotension, and cardiovascular status, antihypertensive therapy, and surgical recovery require urologic supervision.

Rejudgment record. Cross-check applied — Cross-checked the main REACTT report, two secondary reports, and NCT01026818 for single-trial identity, the post-washout primary outcome, treated denominator, on-drug secondary result, and Lilly funding

Scoring profile behind this grade
EndpointPPatient-reported treatment goal - the symptom is the goal
ReplicationR1Single confirmatory trial
IndependenceI0Evidence comes only from manufacturer studies
Effect sizeE0Null
PrecisionC0The confidence interval leaves room for benefit

The scoring table and the verdict agree (D).

Sub-claim grades by effect

This ingredient is marketed for several effects. A single overall grade blends strong and weak claims together, so each effect is graded separately here. The overall grade reflects the strongest disconfirming or core claim.

Effect (sub-claim)GradeBasis
Unassisted erectile-function recovery after withdrawalDOnce daily versus placebo gave OR 1.1 (0.6 to 2.1).
Improved erectile function during nine months on treatmentCOnce-daily treatment gave OR 2.2 (1.2 to 4.0), but this was a secondary on-drug result from one manufacturer trial.

Cross-check — Codex and Claude

This verdict was drafted by Codex through literature review and source-existence checks, cross-checked through blind grading and adversarial audit, and settled by reapplying the methodology boundary rules. Cases with split grades were resolved through rejudgment.
03

Evidence Table

StudyDesignSampleFundingEndpointResultWeight
Study 1International multicenter three-arm randomized double-blind double-dummy phase IV trial141Funded and sponsored by Eli Lilly and Company, with company employees among the authorsUnassisted recovery to IIEF-EF at least 22 after nine months of treatment and six-week washoutOnce daily 20.9%, on demand 16.9%, placebo 19.1%; daily versus placebo OR 1.1 (95% CI 0.6 to 2.1), P=0.675Multiple reports combined as one null manufacturer-funded trial
§

Receipt — 3 References

All 3 cited sources were verified for existence at the original page (as of 2026-08-15).

Montorsi F, Brock G, Stolzenburg JU, Mulhall J, Moncada I, Patel HR, Chevallier D, Krajka K, Henneges C, Dickson R, Büttner H. Effects of tadalafil treatment on erectile function recovery following bilateral nerve-sparing radical prostatectomy: a randomised placebo-controlled study (REACTT). Eur Urol. 2014;65(3):587-596. PMID: 24169081. DOI: 10.1016/j.eururo.2013.09.051. NCT01026818.
checked
Moncada I, de Bethencourt FR, Lledó-García E, Romero-Otero J, Turbi C, Büttner H, Henneges C, Martinez Salamanca JI. Effects of tadalafil once daily or on demand versus placebo on time to recovery of erectile function in patients after bilateral nerve-sparing radical prostatectomy. World J Urol. 2015;33(1):23-30. PMID: 25155034. PMCID: PMC4480825. DOI: 10.1007/s00345-014-1377-3. NCT01026818.
checked
Patel HR, Ilo D, Shah N, Cuzin B, Chadwick D, Andrianne R, Henneges C, Barry J, Hell-Momeni K, Branicka J, Büttner H. Effects of tadalafil treatment after bilateral nerve-sparing radical prostatectomy: quality of life, psychosocial outcomes, and treatment satisfaction results from a randomized, placebo-controlled phase IV study. BMC Urol. 2015;15:31. PMID: 25879460. PMCID: PMC4419565. DOI: 10.1186/s12894-015-0022-9. NCT01026818.
checked
Draft and rewrite: Codex (AI) · Verification: Codex blind grading and adversarial audit · Final adjudication: Claude
Reviewed and approved: Chamgap Editorial Team · Approval date: 2026-08-15 · Corrections: none

Cite this verdict

Once-daily tadalafil x natural erectile rehabilitation after prostatectomy Evidence Grade D card
[Chamgap] Once-daily tadalafil x natural erectile rehabilitation after prostatectomy — Evidence Grade D·28. 3 cited sources checked. Source: https://chamgap.com/en/verdicts/mens/daily-tadalafil-post-prostatectomy-unassisted-erectile-rehabilitation/ · CC BY 4.0

CC BY 4.0 — free to use with attribution; do not distort grades, numbers, or verdict meaning.

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