Visual Analogue Scale
Conditions
Brief summary
In the management of pain after Caesarean section (C/S), opioid or nonsteroidal anti-inflammatory parenteral drugs are applied. These drugs are insufficient in some cases and may cause pain attacks during the day. Higher doses and repeated drug applications or combined drug administration may cause drug side effects and interactions. Alternative applications to provide analgesia include subcutaneous and intracutaneous local anesthetic application to the wound site. Although the effectiveness of these applications has been tested in individuals with different clinical characteristics and has been shown to be largely more successful, they have not been sufficiently introduced into routine practice. There is a need to review the pain methods suggested in the literature and develop new solutions that can be applied more optimally, improve the patient's pain management in the postoperative period, and increase their quality of life and satisfaction. It aims to evaluate the success of subcutaneous and intracutaneous local anesthesia applications compared to traditional applications, and to find the most optimal management.
Interventions
DRUGneural therapy
This prospective study will be conducted with mothers who underwent general anesthesia for labor or elective cesarean delivery and local anesthesia for postoperative pain management during a one-year period following ethical approval.
Sponsors
Haseki Training and Research Hospital
Study design
Observational model
OTHER
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
19 Years to 45 Years
Healthy volunteers
No
Inclusion criteria
* Healthy pregnancy, * Term (\>37 weeks) and preterm (28-34 weeks) pregnancy, * Cases that received general anesthesia for cesarean section, * Cases with and without labor, * Cases with and without obesity, * Cases that had their first or second cesarean section
Exclusion criteria
* Pregnant women under 19 years of age, * Those with a history of allergic reactions to analgesics to be used, * Stillbirth, * Surgical complications during C/S and placement of an abdominal drain, * No head or breech presentation during C/S, * Occiput posterior presentation during C/S, * Anhydramnios and polyhydramnios, * Allergic reactions to the drugs used in the study, alcohol dependence, drug and substance dependence, chronic pain syndrome, neuropathic pain disorder history, * History of clinically significant cardiovascular, pulmonary, hepatic, renal, neurological, psychiatric, metabolic disease.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Visual analogue scale | 48 hours | 1=no pain, 10=worst pain |
Contacts
Primary Contactemine yılmaz güler
Outcome results
None listed