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Tundra lists 2 Bimaxillar Surgery clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.
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NCT07764731
The Effects of Kinesio Tapeing on Facial Swelling Following Bimaxillary Orthognathic Surgery.
The goal of this prospective clinical trial is to evaluate the additive therapeutic efficacy of Kinesio taping combined with routine post-surgical cryotherapy in reducing acute postoperative facial edema and pain in adult patients undergoing bimaxillary orthognathic surgery. The main questions it aims to answer are: Does the application of compression Kinesio taping significantly reduce post-surgical facial edema compared to standard postoperative care alone? Does Kinesio taping provide additional pain relief and functional recovery during the early acute postoperative phase when compared with standard compression taping? Researchers will compare patients receiving bilateral Kinesio taping alongside standard postoperative cryotherapy to a control group receiving standard postoperative cryotherapy alongside standard compression taping to see if Kinesio taping taping provides a superior or additive effect in decreasing edema and alleviating pain. Participants will: Undergo bimaxillary orthognathic surgery under a standardized surgical protocol. Receive routine postoperative cold/cryotherapy application as part of baseline care. Randomly, have Kinesio tape applied immediately postoperatively using a compression taping approach (intervention group) or receive standard rigid compression taping (control group). Undergo standardized facial swelling and pain assessments at pre-determined postoperative follow-up intervals.
Gender: All
Ages: 18 Years - Any
Updated: 2026-08-14
1 state
NCT06933680
Sphenopalatine Ganglion Block in Bimaxillary Orthognathic Surgery
The goal of this clinical trial is to evaluate whether sphenopalatine ganglion (SPG) block helps with intraoperative pain control, reduces postoperative edema, and decreases pain in adults aged 18 to 45 undergoing bimaxillary orthognathic surgery. The main questions it aims to answer are: * Does SPG block help decrease postoperative swelling and pain compared to a sham block? * Does it improve pain control during surgery and reduce opioid use? Researchers will compare patients receiving SPG block to those receiving a sham block to determine if this technique provides better pain relief and reduces postoperative complications. Participants will: * Be 18 to 45 years old and undergo bimaxillary orthognathic surgery. * Be randomly assigned to receive either a SPG block or a sham block before surgery. * Be monitored for 1 month after surgery to assess pain levels, swelling, opioid use, and possible complications.
Gender: All
Ages: 18 Years - 45 Years
Updated: 2025-04-18
1 state