Described here are methods and systems for the manipulation of ovarian tissues. The methods and systems may be used in the treatment of polycystic ovary syndrome (PCOS). The systems and methods may be useful in the treatment of infertility associated with PCOS.

An endoscope including an insertion portion which is provided with a channel to insert a treatment instrument therethrough, an operation portion which is operated the insertion portion, and an operation lever which holds and moves the treatment instrument to transmit force of the operation to the treatment instrument; and an assistant instrument which assists the movement of the treatment instrument, the assistant instrument comprising a flexible tube in which the insertion path is formed to insert the treatment instrument, a coupling portion which is formed so that the channel is coupled to the insertion path, and a holding portion which is attached to the vicinity of the other end of the flexible tube and which holds the operation portion so that the other end of the flexible tube faces toward the side where the operation lever is disposed.

An ablation device having an electrode control system configured to adjust an output of an active electrode and a variable aspiration control system configured to control aspiration in an aspiration system based upon the output of the active electrode is disclosed. In particular, the variable aspiration control system may adjust the aspiration within the aspiration system between at least a zero aspiration setting corresponding to a low ablation power setting and a high aspiration setting corresponding to a high ablation power setting, whereby a plasma field developed at the active electrode at the high ablation power setting is greater than a plasma field developed at the active electrode at the low ablation power setting. By reducing, if not, ceasing the aspiration provided by the aspiration system for the low ablation power setting, the variable aspiration control system is able to reduce the likelihood that the plasma field will be disturbed.

An ablation device having an electrode control system configured to adjust an output of an active electrode and a variable aspiration control system configured to control aspiration in an aspiration system based upon the output of the active electrode is disclosed. In particular, the variable aspiration control system may adjust the aspiration within the aspiration system between at least a zero aspiration setting corresponding to a low ablation power setting and a high aspiration setting corresponding to a high ablation power setting, whereby a plasma field developed at the active electrode at the high ablation power setting is greater than a plasma field developed at the active electrode at the low ablation power setting. By reducing, if not, ceasing the aspiration provided by the aspiration system for the low ablation power setting, the variable aspiration control system is able to reduce the likelihood that the plasma field will be disturbed.

An electrosurgical system includes an electrosurgical generator having active and return terminals, an electrosurgical instrument including an active electrode, a return instrument including a return electrode, an active plug configured to connect to the active terminal of the generator, a return plug configured to connect to the return terminal of the generator, an active cable extending from the return plug to the electro surgical instrument, a return cable extending from the return plug to the return instrument, a connector cable extending from the active plug to the return plug, and a mechanical switch mechanism disposed within the return plug. The mechanical switch mechanism has a disengaged position in which the active plug is electrically disconnected from the active cable and an engaged position in which the active plug is in electrical communication with the active cable.

Systems and methods for treating a patient's mucus hypersecretion condition are disclosed herein. Certain implementations may involve a method for reducing mucus secretion in an upper airway of a patient to treat at least one of post nasal drip or chronic cough. The method may include advancing a treatment delivery portion of an energy-based treatment device into a nostril of the patient. The treatment delivery portion may contact mucosal tissue of the upper airway without piercing the mucosal tissue. The treatment delivery portion may deliver treatment to at least one tissue selected from the group of the mucosal tissue and another tissue underlying the mucosal tissue to modify a property of the at least one tissue and thus treat at least one of post nasal drip or chronic cough in the patient.

Systems and methods for treating a patient's mucus hypersecretion condition are disclosed herein. Certain implementations may involve a method for reducing mucus secretion in an upper airway of a patient to treat at least one of post nasal drip or chronic cough. The method may include advancing a treatment delivery portion of an energy-based treatment device into a nostril of the patient. The treatment delivery portion may contact mucosal tissue of the upper airway without piercing the mucosal tissue. The treatment delivery portion may deliver treatment to at least one tissue selected from the group of the mucosal tissue and another tissue underlying the mucosal tissue to modify a property of the at least one tissue and thus treat at least one of post nasal drip or chronic cough in the patient.

An electrosurgical device: (a) power cable comprising: (i) a primary lead that connects to a first pole of an AC power source and (ii) one or more auxiliary leads; wherein the power cable includes a dual core having the primary lead on a first side and the one or more auxiliary leads on a second side with a web being located between the first side and the second side.

An electrosurgical device: (a) power cable comprising: (i) a primary lead that connects to a first pole of an AC power source and (ii) one or more auxiliary leads; wherein the power cable includes a dual core having the primary lead on a first side and the one or more auxiliary leads on a second side with a web being located between the first side and the second side.

An electrosurgical generator includes: a power supply configured to output a DC waveform; a power converter coupled to the power supply and configured to generate a radio frequency waveform based on the DC waveform; an active terminal coupled to the power converter and configured to couple to a first electrosurgical instrument and a second electrosurgical instrument; at least one sensor coupled to the power converter and configured to sense at least one property of the radio frequency waveform; and a controller coupled to the power converter. The controller is configured to: determine a first impedance associated with a first electrosurgical instrument and a second impedance associated with a second electrosurgical instrument based on the at least one property of the radio frequency waveform; and adjust at least one parameter of the radio frequency waveform based on the first impedance and the second impedance.