Postpartum pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients aged 20-40 years who underwent epidural labor analgesia and voluntarily signed the consent form to participate in this trial; 2. American Society of Anesthesiologists (ASA) grade I.~II; 3.18.5<=BMI<=30; 4. No analgesic drug use within 3 months; 5. No mental disorders, intellectual disabilities and other diseases; 6. No history of drug abuse, drug abuse, or alcoholism; 7. Be able to communicate well and complete relevant questionnaires and questions.
Exclusion criteria
Exclusion criteria: 1. Patients and their families refuse to sign the informed consent form to participate in the trial; 2. ASA level III or above; 3. Previous history of allergy to narcotic drugs, allergy to the active ingredients and excipients of the drugs used; 4. Severe congenital heart disease or abnormal liver and kidney function (ALT<2ULN; SCr <1.5 times baseline, eGFR <25%); 5. Suffering from conscious disorders; 6. History of neurological diseases and mental illness; 7. There is a serious risk of increased blood pressure or intracranial pressure.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual pain score;blood pressure;hreat rate;oxygen saturation;Edinburgh Postnatal Depression Scale (EPDS);Additional analgesic treatment;The perineal condition of the parturient; | — |
Secondary
| Measure | Time frame |
|---|---|
| degree of satisfaction;adverse event;Urination and defecation;Apagar score; | — |
Countries
China
Contacts
Maternal and Child Health Hospital of Hubei Province