Participants in the study will receive either lidocaine hydrochloride or sodium chloride through an intravenous infusion, meaning the substance is delivered directly into a vein. The study period covers the time around the surgery and the first 48 hours after the breathing tube is removed. Various factors such as pain levels, the amount of pain medication used, the length of time spent in the hospital, and the risk of other issues like pneumonia or acute kidney insufficiency will be observed during the recovery process.

The trial involves a comparison between the effects of methylprednisolone and a placebo. Participants will receive an injection of either the medication or a placebo before their surgery. The study is designed to be randomized and double-blinded, meaning neither the participants nor the researchers will know who receives the actual medication or the placebo, ensuring unbiased results.

The purpose of this study is to investigate whether using methylprednisolone can improve recovery after wisdom tooth surgery. Participants will be monitored for changes in swelling, trismus, and pain following their procedure. This research could provide valuable insights into better managing post-operative symptoms and improving patient comfort after dental surgeries.

The purpose of the study is to evaluate how taking amoxicillin, a type of antibiotic, affects the healing process and any complications that might occur after the surgery. The surgery includes two main procedures: guided bone regeneration, which helps to rebuild the bone, and sinus floor elevation, which involves lifting the sinus membrane to make room for the bone graft. The study will compare the outcomes of patients who take amoxicillin with those who do not, to see if the antibiotic helps reduce complications such as pain, swelling, and other discomforts.

Participants in the study will be monitored for any post-surgical issues, such as how well the surgical site heals and whether there are any signs of infection or implant problems. The study aims to gather information on how patients feel after the surgery, including any pain or discomfort they experience, to better understand the benefits of using amoxicillin in these dental procedures.

Participants in the study will receive either the antibiotic Moxilen 500 mg hard capsules, which contains the active ingredient amoxicillin, or a placebo. The purpose of the study is to assess how these treatments affect patient-centered outcomes, such as the level of pain, swelling, and other discomforts experienced after the surgery. The study will monitor these outcomes over a period of time, with specific attention to the first two weeks after the surgery and then at intervals up to six months.

The study will also record any post-surgical complications, such as issues with wound healing, pain, swelling, and the stability of the dental implants. By comparing the effects of the antibiotic to the placebo, the study aims to provide valuable information on the best practices for managing recovery after this type of dental surgery.

During the study, patients will receive either tranexamic acid solution or placebo applied to their surgical wound surfaces. The medication will be given as a single dose during the surgery. The maximum dose used will be 500 mg of tranexamic acid or an equivalent amount of sodium chloride solution as placebo. Both solutions will be applied directly to the wound surface.

The main purpose is to determine if applying tranexamic acid to surgical wounds can reduce the need for additional procedures due to bleeding within 10 days after surgery. The study will also monitor other post-surgical complications such as wound infections, wound rupture, fluid collection (called seroma), and blood clots (called thromboembolic events) for up to 30 days after the surgery.

The treatment involves inhaling the medication, which helps open up the airways in the lungs to make breathing easier. The study will compare two groups of patients – one group receiving the breathing medication and another group not receiving it – to see if there is a difference in breathing complications that develop within 7 days after surgery.

Throughout the study, doctors will monitor patients’ breathing ability, heart function, and overall well-being. They will check for any side effects that might occur from the treatment, such as rapid heartbeat, headaches, or changes in blood sugar levels. The study will also track how patients are doing up to 6 months after their surgery to understand the long-term effects of the treatment.