Patients with painless oocyte retrieval
Conditions
Interventions
Experimental group:High flow oxygen therapy with nasal catheter
Sponsors
The First Affiliated Hospital of USTC Anhui Provincial Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: 1. Women aged 18-55 years; 2. Patients who plan to undergo painless egg retrieval; 3. American Society of Anesthesiologists (ASA) classification I-II; 4. No communication barriers, able to cooperate with intervention implementation; 5. The subjects participated voluntarily and informedly, and signed the informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients who have previously required long-term nasal cannula continuous oxygen supply (home oxygen therapy); 2. Those with a history of severe sleep apnea, lung disease (such as pneumothorax, etc.); 3. Participated in other clinical studies within or within 30 days; 4. Severe nasal congestion, massive epistaxis, recent nasal trauma, recent nasal surgery; 5. Significantly elevated intracranial and skull base fractures; 6. Other circumstances that the researcher considers inappropriate to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse events associated with hypoxia during oocyte retrieval;Vital signs during painless oocyte retrieval;Changes of respiratory phase and respiratory rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Total amount of narcotic drugs;Recovery time;The patients'satisfaction degree; | — |
Countries
China
Contacts
Public ContactZhou Ling
The First Affiliated Hospital of USTC Anhui Provincial Hospital
Outcome results
None listed