Delta Sleep-Inducing Peptide (DSIP) dosage in published studies and labels
These are the doses used for Delta Sleep-Inducing Peptide (DSIP) in FDA labelling and published clinical studies, reported as each source states them, one row per regimen. They describe what was studied or approved for a specific population. They are not a recommendation, and none of them is a dose for any individual.
Research and educational reference only. This is not medical advice, and no figure on this page is a dosing recommendation.
Last checked against primary sources:
Studied regimens and sources
Delta sleep-inducing peptide has been given to humans in a series of small European studies from the late 1980s and 1990s, typically as an intravenous dose around 25 nmol/kg. Those studies are the only human dosing evidence, several of them reported no effect on the endocrine endpoints measured, and no trial has been registered or published since. There is no approved product and no established regimen.
| Human dosing established | Yes |
|---|---|
| Studied dose range | About 25 nmol/kg intravenously (weight-based) |
| Route | Intravenous |
| Frequency | Single administrations in the published studies |
| Duration studied | Short study protocols |
| Evidence level | Limited Human Evidence |
| Last reviewed | 2026-09-05 |
Research-reported dosing
Doses as studied, one row per regimen. Different trials used different regimens; they are listed separately rather than averaged.
| Study / context | Population | Dose | Route | Frequency | Duration | Outcome studied | Source |
|---|---|---|---|---|---|---|---|
| Chronic insomnia study (1992)Clinical trial · Placebo-controlled clinical study | Chronic insomniac patients | 25 nmol/kg body weight | Intravenous | In the afternoon before the 3rd, 4th and 5th night | Three administrations across a sleep-laboratory protocol | Sleep architecture | Effects of delta sleep-inducing peptide on sleep of chronic insomniac patients. Neuropsychobiology. 1992. |
| Endocrine response study (1993)Clinical trial · Controlled endocrine study with a negative result | Human volunteers | Per study protocol | Intravenous | — | — | Growth hormone and other endocrine responses — no influence found | Delta sleep-inducing peptide administration does not influence growth hormone and prolactin secretion. Psychoneuroendocrinology. 1993. |
| Anaesthesia study (2009)Clinical trial · Clinical study | Surgical patients | Per study protocol | Intravenous | — | — | Bispectral index and electroencephalogram changes | Delta sleep-inducing peptide alters bispectral index, the electroencephalogram and heart rate variability when used as an adjunct to isoflurane anaesthesia. Eur J Anaesthesiol. 2009. |
| Opioid detoxification, open clinical trial (1998)Clinical trial · Open clinical trial | Patients undergoing opioid detoxification | Per study protocol | Intravenous | — | — | Withdrawal symptoms | Opioid detoxification with delta sleep-inducing peptide: results of an open clinical trial. J Clin Psychopharmacol. 1998. |
Where sources disagree
- The published human dose is weight-based and intravenous, around 25 nmol/kg. DSIP is sold for subcutaneous injection with fixed protocols commonly quoted at 100–500 mcg; those figures do not come from the published studies and the route differs.
- Several of the human studies are explicitly negative — DSIP did not influence growth hormone, prolactin, or meal-induced ACTH and cortisol responses. Secondary sources frequently cite this literature as support for hormonal or recovery benefits without noting that the measured endpoints did not change.
- The human literature is largely three decades old and was not followed by registered trials. Absence of newer evidence is not evidence of a dose.