Plastic Detox During IVF Treatment
Endocrine Disrupting Chemical Detox: a Practical Method to Decrease Environmental Exposures and an Evaluation of the Impact on in Vitro Fertilization Treatment
Environmental pollutants are present in many aspects of everyday life. Exposures to common household products, such as food packaging and cookware, may affect reproductive health. Many of these environmental toxicants are known as "endocrine disrupting chemicals" because they can interfere with the body's hormone systems. Our study aims to create a guide that explains common sources of environmental toxicants and offer practical steps to reduce exposure. The investigators will evaluate how well participants understand this information and how consistently the intervention is maintained over time.
To assess whether these changes reduce environmental pollutant exposure, the investigators will measure levels of two classes of toxicants within the urine and blood at the beginning, middle and end of the study in patients struggling with infertility that are planning in vitro fertilization (IVF) treatment. The investigators will also measure the same chemicals in follicular fluid (fluid which surrounds developing eggs in the ovary) and seminal fluid (fluid which surrounds the sperm in semen) and compare these levels to samples from similar patients who did not receive the education or make environmental changes. The goal of this project is to determine whether simple changes to reduce exposure to environmental pollutants can lower chemical levels of toxicants in the body and whether this may ultimately impact outcomes for patients undergoing in vitro fertilization.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Abigail Mancuso, MD
- Numéro de téléphone: 319-356-1767
- E-mail: abigail-mancuso@uiowa.edu
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
La description
Inclusion criteria:
- Unexplained infertility diagnosis (no identifiable male or female causes to infertility)
Exclusion criteria:
- Female age 38 years and older
- Male age 45 and older
- Diagnosis of diminished ovarian reserve
- Diagnosis of PCOS/PMOS
- Smoking or drug use in either male and/or female partner
- BMI >40 in either partner
- Patients using donor oocytes/donor sperm/donor embryos
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Plastic Detox
All participants recruited
|
All patients will be provided education on environmental pollutants and provide practical steps to reduce exposure.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Concentration of Bisphenol in urine
Délai: 12 weeks
|
Concentration of bisphenol will be measured in urine for each participant at 0, 6, and 12 weeks.
|
12 weeks
|
|
Concentration of PFAS in blood
Délai: 12 weeks
|
Concentration of PFAS will be measured in blood for each participant at 0, 6, and 12 weeks.
|
12 weeks
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Baseline environmental exposure questionnaire
Délai: 1 week
|
Participants will provide information to quantify their environmental exposures prior to the intervention in the form of a questionnaire.
Questions have been adapted from PACeQ (plastic associated chemicals exposure questionnaire) to assess exposure to diet/food preparation practices, physical environment, and personal care products.
The questionnaire will be delivered electronically.
|
1 week
|
|
Participant perception of educational material questionnaire
Délai: 1 week
|
Participants will assess the effectiveness of the educational material provided in the intervention.
Questionnaire adapted from the Patient Education Materials Assessment Tool (PEMAT).
|
1 week
|
|
Weekly Questionnaire to measure compliance with implementation strategies
Délai: 12 weeks
|
Participants in this study will choose implementation strategies to decrease their environmental exposure based on options provided in the education.
The participants will then provide a weekly summary of their compliance with their chosen implementation strategies in the form of a questionnaire administered electronically.
|
12 weeks
|
|
Concentration of bisphenol in follicular fluid and seminal fluid
Délai: 12 weeks
|
Participants follicular fluid and seminal fluid bisphenol concentration will be compared to a sample of previously banked control specimens.
|
12 weeks
|
|
Concentration of PFAS in follicular fluid and seminal fluid
Délai: 12 weeks
|
Participants follicular fluid and seminal fluid PFAS concentration will be compared to a sample of previously banked control specimens.
|
12 weeks
|
|
Seminal fluid analysis
Délai: 12 weeks
|
Semen sample will be analyzed prior to participants undergoing education on environmental toxins and methods to decrease exposure.
This baseline semen sample will then be compared to semen samples following the 12 week environmental pollutant detox.
Seminal fluid components that will be compared include concentration, motility, morphology, total motile sperm count.
|
12 weeks
|
|
IVF Outcomes
Délai: 45 weeks
|
Compare oocyte yield, fertilization rate, blastulation rate, clinical pregnancy rate, live birth rate to matched patients that did not undergo environmental pollutant detox.
|
45 weeks
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 202606064
- Environmental Fellows Award (Autre subvention/numéro de financement: American Society for Reproductive Medicine)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .