Desmopressin

AApproved (Rx)Bone and endocrine peptide medicines →DDAVPMinirinNocdurna
In one paragraphDesmopressin is a synthetic analogue of the antidiuretic hormone vasopressin that concentrates urine without raising blood pressure. It is approved for diabetes insipidus, bedwetting, nocturia and some bleeding disorders. A Cochrane review of 14 trials found it reduces night-time voids by a little under one per night in men. Its serious risk is hyponatraemia — low blood sodium — in about 7.6% of older adults, which is why sodium is monitored. It is on WADA's list as a masking agent.
Schematic 3D structure of Desmopressin
9 residues · disulfide-bridged vasopressin analogue · schematic
Overall gradeA Established
Human trialsCochrane review (14 RCTs, n=2,966) + decades of use
Outcomes graded4
Last reviewed23 September 2026
EvidenceWhat it isHow it worksUnknownsMolecule & PKRegulationQuestionsReferences

What the human research shows

A well-characterised medicine with a modest benefit and a well-quantified danger. Grade A on certainty; the effect size for nocturia is small, and the sodium risk is the row that matters.

MetabolicCardioMuscleHealingNeuroImmuneSexualSkinAgeing

Evidence profile0–5

  • Metabolic & weight—0.0
  • Cardiovascular—0.0
  • Muscle & growth—0.0
  • Healing & repair—0.0
  • Neuro & sleep—0.0
  • Immune & inflammation—0.0
  • Sexual & hormonal—0.0
  • Skin & appearance—0.0
  • Ageing & longevity—0.0
No benefit outcome for Desmopressin has both human evidence and a measurable effect, so the profile is empty. That is the finding, not a gap in the chart.
OutcomeGradeEffect sizeHuman studiesWhere the evidence comes from
Nocturia (night-time voids)AEstablishedSmallCochrane review, 14 RCTs (n=2,966 men)About 0.85 fewer voids per night at three to twelve months against placebo, with low-quality evidence; little difference at under three months. A separate meta-analysis in women found 0.41 fewer.12
Hyponatraemia (older adults)adverseAEstablishedModerateMeta-analysis, 7 studiesPooled incidence of low sodium 7.6% in older adults treated for nocturia — the reason for sodium checks before and during treatment and for the boxed warning on the US nasal product.3
Central diabetes insipidusAEstablishedLargeDecades of use; the original indicationReplaces the missing hormone; the standard treatment since the 1970s. Older trials, not modern RCTs, but the effect is unambiguous.4
Nocturnal enuresis in childrenAEstablishedModerateCochrane review (2025 update)Reduces wet nights during treatment; relapse on stopping is common, and alarm training has more durable effect.4
AMultiple good human trials, consistentBSome human trials, mostly consistentCFew or weak human studiesDAnimal or anecdotal onlyeffect size · red = adverse

Literature searched to 23 September 2026. Human studies only; animal and cell work informs the mechanism section and nothing else.

Registered trials

ClinicalTrials.gov lists 86 interventional studies naming Desmopressin as an intervention — 53 completed, 7 recruiting, and 15 with results posted to the registry.

A registration is not a result. Anyone can register a study, and many never report — so this list shows what has been attempted, not what has been shown. The graded evidence above is the answer to whether something works.

StudyPhaseStatusParticipantsSponsorResults
1-deamino 8-d-arginine Vasopressin (DDAVP) in Percutaneous Ultrasound-guided Renal BiopsyNCT00748072 · started Aug 2008Phase 4Completed162University of BariPosted
Desmopressin for Bedwetting in Children With SCDNCT04420585 · started Jul 2020Phase 4Terminated8Montefiore Medical CenterPosted
Efficacy and Safety of Desmopressin Melt for the Treatment of NocturiaNCT00477490 · started May 2007Phase 3Completed799Ferring PharmaceuticalsPosted
An Extension Study Investigating the Efficacy and Safety of a Fast-Dissolving ("Melt") Formulation of Desmopressin for the Treatment of Nocturia in AdultsNCT00615836 · started Dec 2007Phase 3Completed554Ferring PharmaceuticalsPosted
Investigation of the Superiority Effect of Orally Disintegrating Desmopressin Tablets to Placebo in Terms of Night Voids Reduction in Nocturia Adult Male PatientsNCT01262456 · started Feb 2011Phase 3Completed395Ferring PharmaceuticalsPosted
Investigation of the Superiority Effect of Desmopressin to Placebo in Terms of Night Voids Reduction in Nocturia Adult Female PatientsNCT01223937 · started Nov 2010Phase 3Completed268Ferring PharmaceuticalsPosted
Study With Two Different Doses of Desmopressin Orally Lyophilisate Tablet With Nocturnal EnuresisNCT01078753 · started Jan 2010Phase 3Completed89Ferring PharmaceuticalsPosted
Study Investigating the Impact Burden of Nocturia Using the Nocturia Impact DiaryNCT01552343 · started Mar 2012Phase 3Completed56Ferring PharmaceuticalsPosted

78 further studies are registered. Participant counts marked * are the sponsor's estimate, not a final enrolment. Source: ClinicalTrials.gov, read directly from the registry and refreshed weekly.

What it is

Desmopressin is vasopressin with two changes — the first amino acid deaminated and the eighth switched to its mirror form — which remove most of the blood-pressure effect and extend the half-life. Made by Ferring since 1972, it comes as tablets, melt tablets, nasal spray and injection.

Its uses split by dose: high doses for bleeding disorders (it releases stored von Willebrand factor), lower doses to concentrate urine.

How it is thought to work

It activates V2 receptors in the kidney's collecting ducts, inserting water channels so that water is reabsorbed and urine becomes concentrated. Take it and keep drinking, and the retained water dilutes blood sodium — the mechanism of the hyponatraemia.

What is still unknown

  • Quality-of-life benefit in nocturia; the Cochrane review found no evidence either way.
  • The best sodium-monitoring schedule for older adults.

The molecule and how long it lasts

Identity
Formula
C46H64N14O12S2
Molecular weight
1069.2 g/mol
CAS number
16679-58-6
PubChem
CID 5311065

PubChem record, read 23 September 2026.

Pharmacokinetics
Route
Intravenous or subcutaneous injection; also tablets, melt tablets and nasal spray
Half-life
About 2.8 hours
Licensed regimen (DDAVP injection)
Haemophilia A / von Willebrand type 1: 0.3 mcg/kg (max 20 mcg) IV over 15-30 min; central diabetes insipidus: 2-4 mcg daily in 1-2 divided doses SC or IV

From the approved product's prescribing information: DDAVP injection prescribing information (DailyMed) The regimen is the label's own wording, reproduced as a regulatory fact.

Regulatory status

European Union
Approved, prescription-only

Nationally authorised products (Minirin, Nocdurna and generics) across member states.

United States
Approved, prescription-only

DDAVP and generics; Nocdurna (2018) and Noctiva nasal spray (2017) for nocturia, the latter with a boxed warning for hyponatraemia.

United Kingdom
Licensed, prescription-only

Licensed for diabetes insipidus, enuresis, nocturia and haemophilia A / von Willebrand disease.

Australia
Registered, Schedule 4

Minirin and generics on the ARTG.

Canada
Authorised, prescription-only

DDAVP and generics.

Sport (WADA)
Prohibited at all times

Listed under S5 (diuretics and masking agents) since 2011, because it dilutes urine and can mask other substances.

Questions people actually ask

Is desmopressin a peptide?
Yes — nine amino acids in a disulfide ring, a modified copy of the hormone vasopressin.
Why is desmopressin banned in sport?
It concentrates urine and lets an athlete drink to dilute a sample, which can hide other substances. WADA lists it as a masking agent, not for any performance effect.
What is the main risk?
Low blood sodium. In older adults treated for nocturia the pooled rate is about 7.6%; severe cases cause confusion and seizures. Sodium is checked before treatment and again after starting.

One page per claimed effect

References

  1. 1
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Change log

  • 2026-09-23Initial publication. Grade A; small nocturia effect, hyponatraemia quantified, WADA S5 status recorded.