- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07802691
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.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Abigail Mancuso, MD
- Numero di telefono: 319-356-1767
- Email: abigail-mancuso@uiowa.edu
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
Accetta volontari sani
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Altro
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Plastic Detox
All participants recruited
|
All patients will be provided education on environmental pollutants and provide practical steps to reduce exposure.
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Concentration of Bisphenol in urine
Lasso di tempo: 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
Lasso di tempo: 12 weeks
|
Concentration of PFAS will be measured in blood for each participant at 0, 6, and 12 weeks.
|
12 weeks
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Baseline environmental exposure questionnaire
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
|
Collaboratori e investigatori
Sponsor
Collaboratori
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 202606064
- Environmental Fellows Award (Altro numero di sovvenzione/finanziamento: American Society for Reproductive Medicine)
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .