20 Participants NeededMy employer runs this trial

Norethindrone Acetate-Ethinyl Estradiol for Oxytocin Deficiency

(Pedi-EVOLVE Trial)

HL
Overseen ByHannah Lamont, PhD
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores whether a combination of oral estrogen and progestin, specifically Norethindrone Acetate-Ethinyl Estradiol, can stimulate the release of oxytocin, a hormone linked to bonding and stress relief, in individuals with certain hormone deficiencies. It includes two groups: those with hypopituitary disease, which affects hormone production, and those with a specific hormone deficiency called AVP-D. Participants will take a single dose of the medication, and researchers will check their hormone levels. This trial suits individuals diagnosed with AVP-D or hypopituitary disease who have stable hormone replacement therapy. As an Early Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants a chance to contribute to groundbreaking medical discoveries.

Will I have to stop taking my current medications?

If you are currently taking estrogen/progestin, you will need to stop for at least 6 weeks before the main study visits. For other medications, there should be no changes within 2 weeks of enrollment or within 5 half-lives of the medication.

Is there any evidence suggesting that this treatment is likely to be safe for humans?

Research has shown that norethindrone acetate and ethinyl estradiol are generally safe for people. These ingredients, commonly found in birth control pills, have been used safely for many years. Other studies have indicated that a single dose of these hormones does not cause significant side effects, and participants did not report major health problems after using them.

However, since this trial is in its early stages, researchers are closely monitoring the treatment's safety. Being in an early phase means limited information exists on its specific effects for oxytocin deficiency. Based on their use in other treatments, these hormones are usually safe. Researchers will carefully watch participants for any new side effects.12345

Why do researchers think this study treatment might be promising for oxytocin deficiency?

Most treatments for oxytocin deficiency focus on directly supplementing oxytocin levels or using oxytocin analogs. However, Norethindrone Acetate-Ethinyl Estradiol offers a fresh approach. Researchers are excited because this combination could potentially regulate hormonal imbalances differently, possibly impacting oxytocin levels in a new way. By targeting the hormonal axis, this treatment might provide benefits beyond just replacing oxytocin, addressing the root causes of deficiency more holistically. This could lead to more comprehensive symptom relief for patients with hypopituitary disease.

What evidence suggests that Norethindrone Acetate-Ethinyl Estradiol might be an effective treatment for oxytocin deficiency?

Research has shown that a combination of two hormones, norethindrone acetate and ethinyl estradiol, might help increase oxytocin levels. Oxytocin plays a crucial role in social connections and emotional regulation. Early findings suggest that this hormone combination could boost oxytocin in individuals with a condition affecting hormone balance. In this trial, participants with hypopituitary disease, both with and without arginine-vasopressin deficiency (AVP-D), will receive norethindrone acetate-ethinyl estradiol to evaluate its effects on oxytocin levels. Previous studies have demonstrated that even a single dose can alter oxytocin levels. However, further research is needed to understand its effectiveness in treating low oxytocin levels.12367

Who Is on the Research Team?

EA

Elizabeth A Lawson, MD

Principal Investigator

Massachusetts General Hospital

Are You a Good Fit for This Trial?

This trial is for children and teens with certain pituitary disorders, like AVP-D or hypopituitarism, who have stable hormone treatments and can speak English. People can't join if they have a history of blood clots, certain cancers, serious heart problems, recent pregnancy or breastfeeding, severe kidney/liver disease, active smoking, or major mental health issues.

Inclusion Criteria

I have AVP-D, stable hormone doses, and can speak English.
I have hypopituitary disease and my hormone doses have not changed in the last 6 weeks.

Exclusion Criteria

I do not have recent serious illnesses, cancer history, or risky medication or lifestyle factors.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive a single administration of norethindrone acetate and ethinyl estradiol, with blood and saliva sampling at baseline and 24 hours post-administration

1 day
2 visits (in-person)

Follow-up

Participants are monitored for changes in neurophysin-1 and oxytocin levels, as well as neuropsychological assessments

1 day

What Are the Treatments Tested in This Trial?

Interventions

  • Norethindrone Acetate-Ethinyl Estradiol

Trial Overview

The study tests whether a single dose of oral estrogen/progestin (norethindrone acetate-ethinyl estradiol) increases oxytocin levels in youth with pituitary conditions compared to controls. Blood and saliva samples are collected before and after the medication.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Individuals with hypopituitary disease with Arginine-vasopressin deficiency (AVP-D).Experimental Treatment1 Intervention
Group II: Individuals with hypopituitary disease (without AVP-D)Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Massachusetts General Hospital

Lead Sponsor

Trials
3,066
Recruited
13,430,000+

Citations

Identifying Oxytocin Deficiency in Pediatric Patients With ...

This study tests the hypothesis that oral estrogen/progestin will stimulate endogenous oxytocin release in control subjects. Eligible ...

Norethindrone Acetate-Ethinyl Estradiol for Oxytocin ...

This trial studies Norethindrone Acetate-Ethinyl Estradiol to determine if it can increase oxytocin levels in individuals with arginine-vasopressin deficiency ...

Identifying Oxytocin Deficiency in Adults With Pituitary ...

This is an open-label, pilot study, to characterize oxytocin response to a single dose of oral Estrogen-progestin in patients with arginine-vasopressin ...

The Oxytocin System and Implications for Oxytocin Deficiency ...

Finally, a study of ethinylestradiol-norethindrone acetate (70 µg and 0.5 mg, respectively) will investigate circulating OXT response in blood and salivary ...

Oxytocin: a neglected hormone in pituitary disease - PMC

While OXT may promote prosocial behavior, its effectiveness across all core ASD symptoms remains uncertain (). Importantly, unlike AVP-Deficiency, no primary ...

Identifying oxytocin deficiency in pituitary disease

We are doing this research to understand whether a single dose of a hormone pill (norethindrone acetate/ethinyl estradiol) could be used to identify ...

Norethindrone Acetate-Ethinyl Estradiol in Hypopituitarism and ...

This study tests the hypothesis that oral estrogen/progestin will stimulate endogenous oxytocin release in control subjects. Eligible participants will receive ...