postoperatival pain
Conditions
Interventions
Laparoscopic treatment group:Multimodal analgesia
the control group of laparoscopic:None
laparotomy treatment group:Multimodal analgesia
the control group of laparotomy:None
Sponsors
Obstetrics and Gynecology Department of the Second Hospital of Anhui Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. gynecological laparoscopy or laparotomy, vaginal surgery patients; 2. aged 18 years old or more.
Exclusion criteria
Exclusion criteria: 1. sodium for injection with parry smoothie cloth active ingredients or excipient in any of the ingredients in patients with a history of allergies; 2. history of serious drug allergy reaction, especially skin reactions, such as eyes, skin and mucosa syndrome (Stevens Johnson syndrome), toxic epidermal necrosis release, erythema multiforme, etc., or known allergic to sulfa drugs; 3. the patients of bronchospasm, acute rhinitis, nasal polyps, angioneurotic oedema, urticaria and other allergic reaction after use aspirin and non-steroidal anti-inflammatory drugs (including cox-2 inhibitors); 4. congestive heart failure (NYHA II - IV); 5. after coronary artery bypass surgery for the treatment of postoperative pain; 6. has determined the ischemic heart disease, peripheral arterial blood vessels and/or cerebrovascular disease; 7. active peptic ulcer or gastrointestinal bleeding; 8. severe liver function damage (serum albumin < 25 g/l or Child - Pugh score 10 or higher); 9. inflammatory bowel disease; 10. pregnant or lactating patients.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score;Anxiety depression score;Postoperative adverse reactions; | — |
Secondary
| Measure | Time frame |
|---|---|
| blood routine examination; | — |
Countries
China
Contacts
Public ContactBing Wei
Obstetrics and Gynecology Department of the Second Hospital of Anhui Medical University
Outcome results
None listed