1987
In chronic insomniacs, DSIP substantially improved night sleep from the first dose and continued improving with repeated treatment. Efficiency of night sleep and daytime rest reached normal levels, and participants showed increased alertness and mental performance during the day.
Schneider-Helmert D
1983
Human studies confirmed DSIP promotes natural sleep with effects lasting up to 20 hours after a single dose. Beyond sleep, DSIP improved daytime alertness, performance, stress tolerance, and coping ability—showing it does much more than just help you fall asleep.
Schneider-Helmert D, Schoenenberger GA
1981
In healthy volunteers, DSIP increased total sleep time by 59% during the day and improved subsequent night sleep quality. Importantly, there was no classic sedation—subjects maintained normal alertness when awake. The compound was well-tolerated with no psychological, physiological, or biochemical side effects.
Graf MV, Kastin AJ
1981
Chronic insomniacs receiving DSIP had longer sleep duration, higher quality sleep with fewer interruptions, and slightly more REM sleep—but no daytime sedation. The sleep-promoting effects lasted up to 6 hours through the night.
Schneider-Helmert D, Schoenenberger GA
2011
DSIP showed strong antioxidant effects in aging rats, switching on the body's natural antioxidant defenses, including superoxide dismutase, catalase and ceruloplasmin (protective enzymes and proteins). This suggests DSIP may have anti-aging benefits beyond better sleep.
Bondarenko TI, Maĭboroda EA, Mikhaleva II
1987
A double-blind crossover study (each patient got both DSIP and placebo, and no one knew which) in chronic insomniacs, 25 nmol/kg intravenously (into a vein) across four nights. Night-time awakenings, time awake and time to fall into non-REM sleep (deep, non-dreaming sleep) all fell on DSIP, but none of those changes was significantly different from the patients' own baseline or from the double-blind placebo nights. Total sleep time and non-REM sleep did rise significantly versus placebo, but the same gap was already present in the baseline values. The authors concluded that the sleep improvement is "of little clinical significance."
Monti JM, Debellis J, Alterwain P, Pellejero T, Monti D
1992
Sixteen chronic insomniacs, double-blind, matched pairs, parallel groups (two matched groups, each getting one treatment), five consecutive nights in a sleep laboratory. Half received 25 nmol/kg DSIP intravenously (into a vein) in the afternoon before nights 3, 4 and 5; half received a glucose placebo. Sleep efficiency (the share of time in bed spent asleep) was higher and sleep latency (time to fall asleep) shorter on DSIP. The authors judged those effects weak, noted they could in part be due to an incidental change in the placebo group, found no change in subjective sleep quality or any other measure, and concluded that short-term DSIP treatment of chronic insomnia is "not likely to be of major therapeutic benefit."
Bes F, Hofman W, Schuur J, Van Boxtel C
1995
The only human study to test DSIP's reported stress-hormone effect directly. Healthy young men received DSIP intravenously (into a vein), in total doses of 3 and 4 mg, against placebo, first around a corticotropin-releasing hormone challenge (a test that triggers a stress-hormone response; 5 men per condition) and then around a midday meal (10 more men). ACTH and cortisol (stress hormone) responses were almost identical on DSIP and on placebo in both experiments. The authors concluded their data "do not support an inhibitory role of DSIP on ACTH and cortisol secretion in man," which is the opposite of what had been reported in cells and in animals.
Spath-Schwalbe E, Schafer A, Uthgenannt D, Born J, Fehm HL